Difference between revisions of "MSigDB Acknowledgements"
Line 24: | Line 24: | ||
<v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | <v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | ||
o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | ||
− | </v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" | + | </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]--> <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> |
<p><!--[if gte vml 1]><v:shape id="_x0000_i1026" type="#_x0000_t75" alt="" | <p><!--[if gte vml 1]><v:shape id="_x0000_i1026" type="#_x0000_t75" alt="" | ||
style='width:12pt;height:4.5pt'> | style='width:12pt;height:4.5pt'> | ||
<v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | <v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | ||
o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | ||
− | </v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" | + | </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]--> <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"> | ||
− | <li | + | <li style="" class="MsoNormal"><span lang="FR" style="">BioCarta: http://www.biocarta.com/<o:p></o:p></span></li> |
− | <li | + | <li style="" class="MsoNormal">Signaling pathway database: http://www.grt.kyushu-u.ac.jp/spad/menu.html</li> |
− | <li | + | <li style="" class="MsoNormal">Signaling gateway: http://www.signaling-gateway.org/</li> |
− | <li | + | <li style="" class="MsoNormal">Signal transduction knowledge environment: http://stke.sciencemag.org/</li> |
− | <li | + | <li style="" class="MsoNormal">Human protein reference database: http://www.hprd.org/</li> |
− | <li | + | <li style="" class="MsoNormal">GenMAPP: http://www.genmapp.org/</li> |
− | <li | + | <li style="" class="MsoNormal">Gene ontology: http://www.geneontology.org/</li> |
− | <li | + | <li style="" class="MsoNormal">Sigmal Aldrich pathways: http://www.sigmaaldrich.com/Area_of_Interest/Biochemicals/Enzyme_Explorer/Key_Resources.html</li> |
− | <li | + | <li style="" class="MsoNormal">Gene arrays, BioScience corporation: http://www.superarray.com/</li> |
− | <li | + | <li style="" class="MsoNormal">Human cancer genome anatomy consortium: http://cgap.nci.nih.gov/</li> |
− | <li | + | <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> | ||
Line 48: | Line 48: | ||
<v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | <v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | ||
o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | ||
− | </v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" | + | </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]--> <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 are catalogued in [http://wwwdev.broad.mit.edu/gsea/doc/xie05_motif_paper.pdf Xie, et al, 2005] <a href="http://www.broad.mit.edu/personal/xhx/publications/xie05_motif_paper.pdf">(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. </a></p> |
<p><!--[if gte vml 1]><v:shape id="_x0000_i1028" type="#_x0000_t75" alt="" | <p><!--[if gte vml 1]><v:shape id="_x0000_i1028" type="#_x0000_t75" alt="" | ||
style='width:12pt;height:4.5pt'> | style='width:12pt;height:4.5pt'> | ||
<v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | <v:imagedata src="file:///C:\DOCUME~1\hkuehn\LOCALS~1\Temp\msohtml1\01\clip_image001.gif" | ||
o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | o:href="http://www.broad.mit.edu/gsea/images/bullet.gif" /> | ||
− | </v:shape><![endif]--><!--[if !vml]--><img width="16" height="6" border="0" | + | </v:shape><![endif]--><!--[if !vml]--><a href="http://www.broad.mit.edu/personal/xhx/publications/xie05_motif_paper.pdf"><img width="16" height="6" border="0" v:shapes="_x0000_i1028" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" /><!--[endif]--> <strong>Database C4, Computed (correlational): </strong>Correlation gene sets are groups of genes defined by computationally mining large-scale experimental datasets for co-expressed genes. </a></p> |
Revision as of 10:57, 31 March 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:
- BioCarta: http://www.biocarta.com/<o:p></o:p>
- Signaling pathway database: http://www.grt.kyushu-u.ac.jp/spad/menu.html
- Signaling gateway: http://www.signaling-gateway.org/
- Signal transduction knowledge environment: http://stke.sciencemag.org/
- Human protein reference database: http://www.hprd.org/
- GenMAPP: http://www.genmapp.org/
- Gene ontology: http://www.geneontology.org/
- Sigmal Aldrich pathways: http://www.sigmaaldrich.com/Area_of_Interest/Biochemicals/Enzyme_Explorer/Key_Resources.html
- Gene arrays, BioScience corporation: http://www.superarray.com/
- Human cancer genome anatomy consortium: http://cgap.nci.nih.gov/
- 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.
<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 <a href="http://www.broad.mit.edu/personal/xhx/publications/xie05_motif_paper.pdf">(and supplemental information) and represent known or likely regulatory elements in promoters and 3'-untranslated regions. </a>
<a href="http://www.broad.mit.edu/personal/xhx/publications/xie05_motif_paper.pdf"><img width="16" height="6" border="0" v:shapes="_x0000_i1028" src="file:///C:%5CDOCUME~1%5Chkuehn%5CLOCALS~1%5CTemp%5Cmsohtml1%5C01%5Cclip_image001.gif" alt="" /> Database C4, Computed (correlational): Correlation gene sets are groups of genes defined by computationally mining large-scale experimental datasets for co-expressed genes. </a>