MSigDB Acknowledgements

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</v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" alt="" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" v:shapes="_x0000_i1025" /><!--[endif]-->&nbsp;&nbsp; <strong>Category C1, Positional (chromosomal location):</strong> Contains 24 gene sets corresponding to the genes on each of the 24 human chromosomes, as well as 301 sets corresponding to cytogenetic bands. These gene sets can be helpful in identifying effects related to epigenetic silencing, dosage compensation, copy number polymorphisms, and aneuploidy or other chromosomal deletions/amplifications. </p>
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</v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" v:shapes="_x0000_i1025" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" /><!--[endif]-->&nbsp;&nbsp; <strong>Category C1, Positional (chromosomal location):</strong> Contains 24 gene sets corresponding to the genes on each of the 24 human chromosomes, as well as 301 sets corresponding to cytogenetic bands. These gene sets can be helpful in identifying effects related to epigenetic silencing, dosage compensation, copy number polymorphisms, and aneuploidy or other chromosomal deletions/amplifications. </p>
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</v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" alt="" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" v:shapes="_x0000_i1026" /><!--[endif]-->&nbsp;&nbsp; <strong>Category C2, Curated (functional):</strong> Contains gene sets of metabolic and signaling pathways gleaned from the following publicly available manually curated databases:</p>
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</v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" v:shapes="_x0000_i1026" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" /><!--[endif]-->&nbsp;&nbsp; <strong>Category C2, Curated (functional):</strong> Contains gene sets of metabolic and signaling pathways gleaned from the following publicly available manually curated databases:</p>
<ol type="1" start="1">
<ol type="1" start="1">
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     <li class="MsoNormal" style=""><span lang="FR" style="">BioCarta: http://www.biocarta.com/<o:p></o:p></span></li>
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     <li style="" class="MsoNormal"><span lang="FR" style="">BioCarta: http://www.biocarta.com/<o:p></o:p></span></li>
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     <li class="MsoNormal" style="">Signaling pathway database:      http://www.grt.kyushu-u.ac.jp/spad/menu.html</li>
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     <li style="" class="MsoNormal">Signaling pathway database:      http://www.grt.kyushu-u.ac.jp/spad/menu.html</li>
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     <li class="MsoNormal" style="">Signaling gateway:      http://www.signaling-gateway.org/</li>
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     <li style="" class="MsoNormal">Signaling gateway:      http://www.signaling-gateway.org/</li>
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     <li class="MsoNormal" style="">Signal transduction knowledge      environment: http://stke.sciencemag.org/</li>
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     <li style="" class="MsoNormal">Signal transduction knowledge      environment: http://stke.sciencemag.org/</li>
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     <li class="MsoNormal" style="">Human protein reference      database: http://www.hprd.org/</li>
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     <li style="" class="MsoNormal">Human protein reference      database: http://www.hprd.org/</li>
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     <li class="MsoNormal" style="">GenMAPP:      http://www.genmapp.org/</li>
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     <li style="" class="MsoNormal">GenMAPP:      http://www.genmapp.org/</li>
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     <li class="MsoNormal" style="">Gene ontology:      http://www.geneontology.org/</li>
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     <li style="" class="MsoNormal">Gene ontology:      http://www.geneontology.org/</li>
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     <li class="MsoNormal" style="">Sigmal Aldrich pathways:      http://www.sigmaaldrich.com/Area_of_Interest/Biochemicals/Enzyme_Explorer/Key_Resources.html</li>
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     <li style="" class="MsoNormal">Sigmal Aldrich pathways:      http://www.sigmaaldrich.com/Area_of_Interest/Biochemicals/Enzyme_Explorer/Key_Resources.html</li>
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     <li class="MsoNormal" style="">Gene arrays, BioScience      corporation: http://www.superarray.com/</li>
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     <li style="" class="MsoNormal">Gene arrays, BioScience      corporation: http://www.superarray.com/</li>
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     <li class="MsoNormal" style="">Human cancer genome anatomy      consortium: http://cgap.nci.nih.gov/</li>
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     <li style="" class="MsoNormal">Human cancer genome anatomy      consortium: http://cgap.nci.nih.gov/</li>
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     <li class="MsoNormal" style="">L2L, John Newman and Alan      Weiner, Department of Biochemistry, <st1:place w:st="on"><st1:placetype w:st="on">University</st1:placetype> of <st1:placename w:st="on">Washington</st1:placename></st1:place>. http://depts.washington.edu/l2l/</li>
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     <li style="" class="MsoNormal">L2L, John Newman and Alan      Weiner, Department of Biochemistry, <st1:place w:st="on"><st1:placetype w:st="on">University</st1:placetype> of <st1:placename w:st="on">Washington</st1:placename></st1:place>. http://depts.washington.edu/l2l/</li>
</ol>
</ol>
<p>In addition, contains gene sets representing gene expression signatures of genetic and chemical perturbations that have been culled from experimental results in the literature.</p>
<p>In addition, contains gene sets representing gene expression signatures of genetic and chemical perturbations that have been culled from experimental results in the literature.</p>
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</v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" alt="" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" v:shapes="_x0000_i1027" /><!--[endif]-->&nbsp;&nbsp; <strong>Database C3, Motif (motif-based):</strong> Each gene set in this category contains genes that lie downstream of a motif that is conserved across the human, mouse, rat, and dog genomes. The motifs <span style="font-family: Arial;">are catalogued in [http://wwwdev.broad.mit.edu/gsea/doc/xie05_motif_paper.pdf Xie, et al, 2005] and [http://wwwdev.broad.mit.edu/gsea/doc/xie05_motif_paper_supp_info.pdf Supplemental Information] and represent known or likely regulatory elements in promoters and 3'-untranslated regions.</span></p>
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</v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" v:shapes="_x0000_i1027" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" /><!--[endif]-->&nbsp;&nbsp; <strong>Database C3, Motif (motif-based):</strong> Each gene set in this category contains genes that lie downstream of a motif that is conserved across the human, mouse, rat, and dog genomes. The motifs <span style="font-family: Arial;">are catalogued in [http://wwwdev.broad.mit.edu/gsea/doc/xie05_motif_paper.pdf Xie, et al, 2005] and [http://wwwdev.broad.mit.edu/gsea/doc/xie05_motif_paper_supp_info.pdf Supplemental Information] and represent known or likely regulatory elements in promoters and 3'-untranslated regions. Please cite Xie <span style="font-style: italic;">et al</span> if using this database.<br /></span></p>
<p><strong>Database C4, </strong>Computed (correlational): Correlation gene sets are groups of genes defined by computationally mining large-scale experimental datasets for co-expressed genes built from the neighborhoods of ~400 cancer related genes (seeds).<span style="font-family: Arial;"></span></p>
<p><strong>Database C4, </strong>Computed (correlational): Correlation gene sets are groups of genes defined by computationally mining large-scale experimental datasets for co-expressed genes built from the neighborhoods of ~400 cancer related genes (seeds).<span style="font-family: Arial;"></span></p>
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<p><span style="font-size: 12pt; font-family: &quot;Times New Roman&quot;;"><img width="16" height="6" alt="" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" v:shapes="_x0000_i1025" /><!--[endif]--> <span style="font-weight: bold;"></span></span></p>
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Revision as of 16:36, 7 April 2006

The Molecular Signature Database (MSigDB) is a collection of gene sets maintained by the GSEA team. The team welcomes and appreciates contributions to this shared resource and encourages users to submit their gene sets to mailto:gsea@broad.mit.edu. The MSigDB contains four categories of genes sets. Our thanks to the contributors.

<img width="16" height="6" border="0" v:shapes="_x0000_i1025" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" />   Category C1, Positional (chromosomal location): Contains 24 gene sets corresponding to the genes on each of the 24 human chromosomes, as well as 301 sets corresponding to cytogenetic bands. These gene sets can be helpful in identifying effects related to epigenetic silencing, dosage compensation, copy number polymorphisms, and aneuploidy or other chromosomal deletions/amplifications.

<img width="16" height="6" border="0" v:shapes="_x0000_i1026" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" />   Category C2, Curated (functional): Contains gene sets of metabolic and signaling pathways gleaned from the following publicly available manually curated databases:

  1. BioCarta: http://www.biocarta.com/<o:p></o:p>
  2. Signaling pathway database: http://www.grt.kyushu-u.ac.jp/spad/menu.html
  3. Signaling gateway: http://www.signaling-gateway.org/
  4. Signal transduction knowledge environment: http://stke.sciencemag.org/
  5. Human protein reference database: http://www.hprd.org/
  6. GenMAPP: http://www.genmapp.org/
  7. Gene ontology: http://www.geneontology.org/
  8. Sigmal Aldrich pathways: http://www.sigmaaldrich.com/Area_of_Interest/Biochemicals/Enzyme_Explorer/Key_Resources.html
  9. Gene arrays, BioScience corporation: http://www.superarray.com/
  10. Human cancer genome anatomy consortium: http://cgap.nci.nih.gov/
  11. L2L, John Newman and Alan Weiner, Department of Biochemistry, <st1:place w:st="on"><st1:placetype w:st="on">University</st1:placetype> of <st1:placename w:st="on">Washington</st1:placename></st1:place>. http://depts.washington.edu/l2l/

In addition, contains gene sets representing gene expression signatures of genetic and chemical perturbations that have been culled from experimental results in the literature.

Several colleagues have contributed to this effort, including:

Jean-Pierre Bourquin (Orkin lab)
Ben Ebert (Golub lab)
Yujin Hoshida (Golub lab)
Jean Junior (Student)
John Newman (L2L, Washington University)
Kate Stafford (MIT, UROP)
Lisa Sturla (Pomeroy lab)

Please see the annotation of a gene set in its GeneSetCard or the MSigDB Browser included in the GSEA java desktop application for the source/contributor of a gene set.

<img width="16" height="6" border="0" v:shapes="_x0000_i1027" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" />   Database C3, Motif (motif-based): Each gene set in this category contains genes that lie downstream of a motif that is conserved across the human, mouse, rat, and dog genomes. The motifs are catalogued in Xie, et al, 2005 and Supplemental Information and represent known or likely regulatory elements in promoters and 3'-untranslated regions. Please cite Xie et al if using this database.

Database C4, Computed (correlational): Correlation gene sets are groups of genes defined by computationally mining large-scale experimental datasets for co-expressed genes built from the neighborhoods of ~400 cancer related genes (seeds).

<img width="16" height="6" alt="" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" v:shapes="_x0000_i1025" />


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