<?xml version="1.0"?><?xml-stylesheet type="text/xsl" href="/rss.xsl"?><rss version="2.0"><channel><title>MSCompBio Wiki &amp; Documentation Rss Feed</title><link>http://www.codeplex.com/MSCompBio/Wiki/View.aspx?title=Home</link><description>MSCompBio Wiki Rss Description</description><item><title>Updated Wiki: Home</title><link>https://mscompbio.codeplex.com/wikipage?version=46</link><description>&lt;div class="wikidoc"&gt;
&lt;h2&gt;Project Description&lt;/h2&gt;
&lt;p&gt;Computational biology tools from Microsoft Research's eScience group: PhyloD (Phylogeny-Based Association Analysis), Epitope Prediction, HLA Assignment, HLA Completion&lt;br&gt;
&lt;br&gt;
&lt;/p&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;
&lt;p&gt;&lt;em&gt;Different tools have difference licenses. Check each tool's license individually.&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/Fastlmm/"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over
 120,000 individuals. &lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/Fastlmm/"&gt;FaST-LMM-Set &amp;nbsp;&amp;nbsp;
&lt;span style="color:#0000de"&gt;-- COMING SOON --&lt;/span&gt;&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;FaST-LMM-Set extends the capabilities of FaST-LMM to handle associations between sets of variants and phenotype.
&lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity.
&lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to &amp;ldquo;escape&amp;rdquo;
 the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called
 epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA. This evolution takes place
 anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes. PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the
 virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the
 virus is unable to develop resistance. &lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele. The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.
&lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;HLA sequence typing sometimes yields uncertain results. For example, an allele may be identified as A6801/6802 or simply A02. This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically
 &amp;ldquo;completes&amp;rdquo; the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT. One problem with this approach is that, if you see a reaction in a patient, you don&amp;rsquo;t know which of the patient&amp;rsquo;s HLA genes is responsible for the reaction. This tool takes lab data
 from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.
&lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.
&lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;
&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher's statistics.
&lt;/li&gt;&lt;/ul&gt;
&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;
&lt;p&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br&gt;
&lt;a href="/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/&lt;/a&gt;&lt;/p&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;
&lt;p&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;/p&gt;
&lt;h2&gt;Microsoft Research's eScience Research Group&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;
&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;General Practical Information&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;&lt;a href="/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;
&lt;/li&gt;&lt;li&gt;&lt;a href="/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;&lt;br&gt;
&lt;br&gt;
&lt;br&gt;
&lt;img title="masthead.png" src="http://i3.codeplex.com/Download?ProjectName=mscompbio&amp;DownloadId=8894" alt="masthead.png"&gt;&lt;/p&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>bobd00</author><pubDate>Sat, 20 Apr 2013 01:06:42 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20130420010642A</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=45</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;
&lt;i&gt;Different tools have difference licenses. Check each tool&amp;#39;s license individually.&lt;/i&gt;&lt;br /&gt;
&lt;ul&gt;&lt;li&gt;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/Fastlmm/"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt; eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>CarlK</author><pubDate>Thu, 14 Jun 2012 23:10:07 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120614111007P</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=44</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;
&lt;i&gt;Different tools have difference licenses. Check each tools license individually.&lt;/i&gt;&lt;br /&gt;
&lt;ul&gt;&lt;li&gt;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/Fastlmm/"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt; eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>CarlK</author><pubDate>Thu, 14 Jun 2012 23:09:48 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120614110948P</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=43</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/Fastlmm/"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt; eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>CarlK</author><pubDate>Thu, 14 Jun 2012 21:48:58 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120614094858P</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=42</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/#fastlmm"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt; eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>CarlK</author><pubDate>Thu, 14 Jun 2012 19:08:04 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120614070804P</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=41</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt; eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>CarlK</author><pubDate>Thu, 14 Jun 2012 19:07:34 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120614070734P</guid></item><item><title>Updated Wiki: eLMM</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;version=7</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Code&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;/strong&gt;Executables&amp;nbsp;are available &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;
here&lt;/a&gt;&amp;nbsp;and source code is available by going to &lt;a href="http://mscompbio.codeplex.com/SourceControl/list/changesets"&gt;
here&lt;/a&gt;&amp;nbsp;and using the Browse Tab to search for eLMM.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Paper&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History: &lt;/strong&gt;&lt;a href=" http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt"&gt;here&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 03:05:26 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM 20120522030526A</guid></item><item><title>Updated Wiki: eLMM</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;version=6</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Code&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;/strong&gt;Executables&amp;nbsp;are available &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;
here&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Paper&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History: &lt;/strong&gt;&lt;a href=" http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt"&gt;here&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>CarlK</author><pubDate>Tue, 22 May 2012 03:00:39 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM 20120522030039A</guid></item><item><title>Updated Wiki: eLMM</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;version=5</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Code&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;/strong&gt;Executables is available &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;
here&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Paper&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History: &lt;/strong&gt;&lt;a href=" http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt"&gt;here&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 02:59:06 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM 20120522025906A</guid></item><item><title>Updated Wiki: eLMM</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;version=4</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Code&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;/strong&gt;A combination of C# source code and executables is available &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;
here&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Paper&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History: &lt;/strong&gt;&lt;a href=" http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt"&gt;here&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:16:36 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM 20120522011636A</guid></item><item><title>Updated Wiki: eLMM</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;version=3</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Code&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;/strong&gt;A combination of C# source code and executables is available &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;
here&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Paper&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.genomeweb.com/informatics/microsoft-research-led-team-develops-method-correct-confounders-eqtl-analyses"&gt;GenomeWeb
 coverage&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History:&amp;nbsp;&lt;/strong&gt;http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:13:47 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM 20120522011347A</guid></item><item><title>Updated Wiki: eLMM</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;version=2</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;Code is available at: [url:http://mscompbio.codeplex.com/downloads/get/381554] (Combination of C# source code and executables)&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.genomeweb.com/informatics/microsoft-research-led-team-develops-method-correct-confounders-eqtl-analyses"&gt;GenomeWeb
 coverage&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History:&amp;nbsp;&lt;/strong&gt;http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:12:51 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM 20120522011251A</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=40</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://fastlmm.codeplex.com"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt; eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:11:46 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120522011146A</guid></item><item><title>Updated Wiki: eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;version=2</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.genomeweb.com/informatics/microsoft-research-led-team-develops-method-correct-confounders-eqtl-analyses"&gt;GenomeWeb
 coverage&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History:&amp;nbsp;&lt;/strong&gt;http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;br&gt;
&lt;/strong&gt;&lt;/p&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:10:54 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) 20120522011054A</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=39</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://fastlmm.codeplex.com"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;referringTitle=Home"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Code: &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;http://mscompbio.codeplex.com/downloads/get/381554&lt;/a&gt; (Combination of C# source code and executables)&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:10:29 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120522011029A</guid></item><item><title>Updated Wiki: eLMM</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM&amp;version=1</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.genomeweb.com/informatics/microsoft-research-led-team-develops-method-correct-confounders-eqtl-analyses"&gt;GenomeWeb
 coverage&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History:&amp;nbsp;&lt;/strong&gt;http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:10:16 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM 20120522011016A</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=38</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://fastlmm.codeplex.com"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=eLMM%20%28Eliminate%20Confouding%20in%20eQTL%20studies%20with%20Linear%20Mixed%20Models%29&amp;referringTitle=Home"&gt;eLMM &amp;#40;Eliminate Confouding in eQTL studies with Linear Mixed Models&amp;#41;&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Code: &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;http://mscompbio.codeplex.com/downloads/get/381554&lt;/a&gt; (Combination of C# source code and executables)&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:09:11 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120522010911A</guid></item><item><title>Updated Wiki: eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)</title><link>http://mscompbio.codeplex.com/wikipage?title=eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;version=1</link><description>&lt;div class="wikidoc"&gt;
&lt;p&gt;&lt;strong&gt;Project Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models)&amp;nbsp;is a program for performing eQTL analysis in the presence of two confounders: (1) population structure, (2) expression heterogeneity&lt;/p&gt;
&lt;p&gt;eLMM is described more fully in the&amp;nbsp;paper&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Correction for Hidden Confounders in the Genetic Analysis of Gene Expression&amp;nbsp;&lt;br&gt;
Jennifer Listgarten, Carl Kadie, Eric Schadt, David Heckerman&amp;nbsp;&lt;br&gt;
&lt;em&gt;Proceedings of the National Academy of Sciences,&amp;nbsp;&lt;/em&gt;September 1, 2010,&amp;nbsp;&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.abstract"&gt;doi: 10.1073/pnas.1002425107&amp;nbsp;&lt;/a&gt;&lt;br&gt;
(&lt;a href="http://www.pnas.org/content/early/2010/08/30/1002425107.full.pdf&amp;#43;html"&gt;paper&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.pnas.org/content/suppl/2010/09/01/1002425107.DCSupplemental/Appendix.pdf"&gt;Supplementary Information&lt;/a&gt;,&amp;nbsp;&lt;a href="http://www.genomeweb.com/informatics/microsoft-research-led-team-develops-method-correct-confounders-eqtl-analyses"&gt;GenomeWeb
 coverage&lt;/a&gt;)&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Version History:&amp;nbsp;&lt;/strong&gt;http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/versionHistory.txt&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;List of mouse associations from the paper:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;&lt;a href="http://research.microsoft.com/en-us/um/redmond/projects/MSCompBio/MSLMM/Top10Khits.txt"&gt;list of the top 10K SNP-gene eQTL associations&amp;nbsp;&lt;/a&gt;found using the LMM-EH-PS model, from the PNAS paper.
&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;br&gt;
&lt;/strong&gt;&lt;/p&gt;
&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 01:08:06 GMT</pubDate><guid isPermaLink="false">Updated Wiki: eLMM (Eliminate Confouding in eQTL studies with Linear Mixed Models) 20120522010806A</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=37</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://fastlmm.codeplex.com"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://eLMM"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Code: &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;http://mscompbio.codeplex.com/downloads/get/381554&lt;/a&gt; (Combination of C# source code and executables)&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>jennl</author><pubDate>Tue, 22 May 2012 00:56:17 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120522125617A</guid></item><item><title>Updated Wiki: Home</title><link>http://mscompbio.codeplex.com/wikipage?version=36</link><description>&lt;div class="wikidoc"&gt;&lt;h2&gt;Project Description&lt;/h2&gt;Computational biology tools from Microsoft Research&amp;#39;s eScience group&amp;#58; PhyloD &amp;#40;Phylogeny-Based Association Analysis&amp;#41;, Epitope Prediction, HLA Assignment, HLA Completion&lt;br /&gt;&lt;br /&gt;
&lt;h2&gt;The Tools&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://fastlmm.codeplex.com"&gt;FaST-LMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;FaST-LMM (Factored Spectrally Transformed Linear Mixed Models) is a program for performing genome-wide association studies (GWAS) on large data sets. Versions of FaST-LMM run on either Windows or Linux systems and have been tested on data sets with over 120,000 individuals.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://eLMM"&gt;eLMM&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Precompiled: &lt;a href="http://mscompbio.codeplex.com/downloads/get/381554"&gt;http://mscompbio.codeplex.com/downloads/get/381554&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=PhyloD&amp;referringTitle=Home"&gt;PhyloD&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Pathogens live and reproduce inside the human host, whose immune system continually tries to rid the body of these pathogens. This leads to a tug-of-war between the pathogen and the human host, where the pathogen tries to adapt so as to “escape” the immune system, while the immune system learns to recognize and eliminate new foreign pathogens. A set of key players for the immune system are the HLA proteins, each of which can recognize specific short fragments of foreign (e.g. HIV) proteins, called epitopes, in infected cells and then alert the immune system to their presence. For rapidly evolving pathogens like HIV, a key defense mechanism is to evolve mutations that prevent the HLA proteins from recognizing the viral DNA.  This evolution takes place anew in each patient, as each patient has a different set of HLA proteins that recognize different epitopes.  PhyloD is a statistical tool that can identify HIV mutations that defeat the function of the HLA proteins in certain patients, thereby allowing the virus to escape elimination by the immune system. By applying this tool to large studies of infected patients, researchers are now able to start decoding the complex rules that govern the HIV mutations, in the hope of one day creating a vaccine to which the virus is unable to develop resistance.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Epitope%20Prediction&amp;referringTitle=Home"&gt;Epitope Prediction&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool computes the probability that a given kmer is a T-cell epitope restricted to a given HLA allele.  The tool can scan for 8, 9, 10, and 11mer epitopes and over all common HLA alleles.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Hla%20Completion&amp;referringTitle=Home"&gt;HLA Completion&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;HLA sequence typing sometimes yields uncertain results.  For example, an allele may be identified as A6801/6802 or simply A02.  This tool takes as input HLA typing data (loci A,B,C) and probabilistically resolves the typing ambiguities (i.e., probabilistically “completes” the data to 4-digit resolution). &lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=HLA%20Assignment&amp;referringTitle=Home"&gt;HLA Assignment&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;One way to find epitopes is to do lab studies such as ELISPOT.  One problem with this approach is that, if you see a reaction in a patient, you don’t know which of the patient’s HLA genes is responsible for the reaction.  This tool takes lab data from a series of patients and determines (probabilistically) which HLA genes are responsible for the reaction.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Create%20Epitome&amp;referringTitle=Home"&gt;Create Epitome&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;This tool takes, as input, a weighted list of amino acid sequences. It creates epitomes of all lengths.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=False%20Discovery%20Rate&amp;referringTitle=Home"&gt;False Discovery Rate&lt;/a&gt;
&lt;ul&gt;&lt;li&gt;Estimate the false discovery rate for 2X2 contingency tables, based on Fisher&amp;#39;s statistics.&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;h2&gt;Web Versions of the Tools&lt;/h2&gt;&lt;a href="http://atom.research.microsoft.com/bio/"&gt;http://atom.research.microsoft.com/bio/&lt;/a&gt;&lt;br /&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=http%3a%2f%2fresearch.microsoft.com%2fen-us%2fum%2fredmond%2fprojects%2fMSCompBio%2f&amp;referringTitle=Home"&gt;http&amp;#58;&amp;#47;&amp;#47;research.microsoft.com&amp;#47;en-us&amp;#47;um&amp;#47;redmond&amp;#47;projects&amp;#47;MSCompBio&amp;#47;&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Pre-Compiled Programs for Windows&lt;/h2&gt;&lt;a href="http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx"&gt;http://www.codeplex.com/MSCompBio/Release/ProjectReleases.aspx&lt;/a&gt;&lt;br /&gt;
&lt;h2&gt;Microsoft Research&amp;#39;s eScience Research Group&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;Group web page &lt;a href="http://research.microsoft.com/research/eScience/"&gt;http://research.microsoft.com/research/eScience/&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;

&lt;h2&gt;General Practical Information&lt;/h2&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Downloading%20and%20compiling%20source%20code&amp;referringTitle=Home"&gt;Downloading and compiling source code&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href="http://mscompbio.codeplex.com/wikipage?title=Why%2032-bit&amp;referringTitle=Home"&gt;Why 32-bit&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;
&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;img src="http://i3.codeplex.com/Download?ProjectName=MSCompBio&amp;DownloadId=8894" alt="masthead.png" title="masthead.png" /&gt;&lt;br /&gt;&lt;/div&gt;&lt;div class="ClearBoth"&gt;&lt;/div&gt;</description><author>CarlK</author><pubDate>Mon, 21 May 2012 23:30:27 GMT</pubDate><guid isPermaLink="false">Updated Wiki: Home 20120521113027P</guid></item></channel></rss>