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| − | <a href="http://www.broadinstitute.org/gsea/">GSEA Home</a> |
| + | [http://www.broadinstitute.org/gsea/ GSEA Home] | |
| − | <a href="http://www.broadinstitute.org/gsea/downloads.jsp">Downloads</a> |
| + | [http://www.broadinstitute.org/gsea/downloads.jsp Downloads] | |
| − | <a href="http://www.broadinstitute.org/gsea/msigdb/">Molecular Signatures Database</a> |
| + | [http://www.broadinstitute.org/gsea/msigdb/ Molecular Signatures Database] | |
| − | [[Main_Page|Documentation]] | | + | [http://www.broadinstitute.org/cancer/software/gsea/wiki/index.php/Main_Page Documentation] | |
| − | <a href="http://www.broadinstitute.org/gsea/contact.jsp">Contact</a>
| + | [http://www.broadinstitute.org/gsea/contact.jsp Contact]<br> |
| − | <br>
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| − | <br>
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| − | <p>This page provides detailed descriptions of all collections of gene sets in MSigDB.</p>
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| − | <p>To learn about changes and other information specific for a particular release of MSigDB, please refer to the corresponding [[Release_Notes]].</p>
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| − | <h2>H: Hallmarks</h2>
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| − | <p>some text</p>
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| − | <h2>C1: positional gene sets</h2>
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| − | <p>Genes from the same genomic location (chromosome or cytogenetic band) are grouped in a gene set. Cytogenetic annotations are from three sources:</p>
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| − | <ol>
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| − | <li>[http://www.genenames.org Human Genome Organization (HUGO) Gene Nomenclature Committee (HGNC)]</li>
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| − | <li>[http://www.ncbi.nlm.nih.gov/unigene/ UniGene]</li>
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| − | <li>[http://www.affymetrix.com Affymetrix] microarray annotations</li>
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| − | </ol>
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| − | <p>We merged the relevant annotations from these resources and derived a single cytogenetic band location for every gene symbol. These were then grouped into sets. Decimals in cytogenetic bands were ignored. For example, 5q31.1 was considered 5q31. Therefore, genes annotated as 5q31.2 and those annotated as 5q31.3 were both placed in the same set, 5q31.</p>
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| − | <p>When there were conflicts, the UniGene entry was used.</p>
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| − | <p>These sets are helpful in identifying effects related to chromosomal deletions or amplifications, dosage compensation, epigenetic silencing, and other regional effects.</p>
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| − | | + | <p> |
| − | <h2>C2: curated gene sets</h2> | + | See the [http://software.broadinstitute.org/gsea/msigdb/collections.jsp MSigDB Collections page] on the main website. |
| − | Gene sets collected from various sources such as online pathway databases, scientific publications and personal contributions from domain experts.
| + | </p> |
| − | <h3>CGP: chemical and genetic perturbations</h3>
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| − | Gene sets represent expression signatures of genetic and chemical perturbations. A number of these gene sets come in pairs: an xxx_UP (xxx_DN) gene set representing genes induced (repressed) by the perturbation. The majority of CGP sets were curated from publications and include links to the [http://www.ncbi.nlm.nih.gov/pubmed PubMed] citation, the exact source of the set (e.g., Table 1) and links to the corresponding raw data in [http://www.ncbi.nlm.nih.gov/geo/ GEO] or [http://www.ebi.ac.uk/arrayexpress/ ArrayExpress] repositories. When the set involves a genetic perturbation, brief description includes a link to the gene's entry in the NCBI [http://www.ncbi.nlm.nih.gov/gene Entrez Gene] database. When the set involves a chemical perturbation, brief description includes a link to the chemical's entry in the NCBI [ PubChem Compound] database.
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| − | <ul>
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| − | <li>Sets curated from biomedical literature by MSigDB team</li>
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| − | <li>Sets kindly shared by the [http://depts.washington.edu/l2l/ L2L] database of published microarray gene expression data (described in [http://genomebiology.com/2005/6/9/R81 Newman and Weiner]). These sets list John Newman as the contributor.</li>
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| − | <li>Sets contributed by Dr. Chi Dang from the [http://www.myccancergene.org/site/mycTargetDB.asp MYC Target Gene Database].</li>
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| − | <li>Individual gene set compilations contributed by MSigDB collaborators. These sets usually are not based on any specific publication.</li>
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| − | </ul>
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| − | <h3>CP: canonical pathways</h3>
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| − | Gene sets from the pathway databases. Usually, these gene sets are canonical representations of a biological process compiled by domain experts.
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| − | <h2>C3: motif gene sets</h2>
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| − | <p>Gene sets group genes by <i>cis</i>-regulatory motifs. The motifs are catalogued in [http://www.nature.com/nature/journal/v434/n7031/abs/nature03441.html Xie et al.] and represent known or putative conserved regulatory elements in promoters and 3’-UTR regions. These sets make it possible to link changes in a genomic experiment to a conserved, putative cis-regulatory elements.</p>
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| − | <h4>Transcription factor targets (TFT)</h4>
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| − | <p>These sets share upstream cis-regulatory motifs which can function as potential transcripton factor binding sites. We used two approaches to generate these gene sets.</p>
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| − | <p>We extracted 460 mammalian transcriptional regulatory motifs from v7.4 [http://www.gene-regulation.com/ TRANSFAC] database. We then generated the motif gene sets consisting of the inferred target genes for each motif. Every such set consists of human genes whose promoters (defined as regions -2kb to +2kb around transcription start site) contain at least one instance of the motif. We named these sets by the corresponding TRANSFAC matrix identifiers, e.g., V$MIF1_01. The set’s full description is the TRANSFAC entry for the matching matrix, in a format described [http://www.gene-regulation.com/pub/databases/transfac/doc/matrix1SM.html here].</p>
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| − | <p>Motif gene sets of ‘conserved instances’ consist of the inferred target genes for each motif <strong>m</strong> of 174 upstream motifs highly conserved among five mammalian species. The motifs are catalogued in [http://www.ncbi.nlm.nih.gov/pubmed/15735639 Xie, et al. (2005, Nature 434, 338–345)] and represent potential transcription factor binding sites. Each motif gene set consists of all human genes whose promoters (defined as regions -kb to +2kb around transcription start site) contained at least one conserved instance of motif <strong>m</strong>. If the motif’s sequence matched a transcription factor binding site documented in the TRANSFAC database (see above), then we appended the name of the TRANSFAC binding matrix to the motif sequence in the gene name, e.g.: MOTIFSEQ_FOO, where MOTIFSEQ is the sequence of motif m and FOO is the TRANSFAC matrix name (e.g., V$MIF1_01). The set’s full description in this case is the TRANSFAC entry for the matching matrix. If the motif’s sequence matched no transcription factor binding site from TRANSFAC v.7.4, then we named the set as MOTIFSEQ_UNKNOWN where MOTIFSEQ is the sequence of motif <strong>m</strong>.</p>
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| − | <h2>C4: computational gene sets</h2>
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| − | <p>Gene sets defined by mining large collections of cancer-oriented genes.</p>
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| − | <h2>C5: GO gene sets</h2>
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| − | <p>Gene sets are named by [http://www.geneontology.org Gene Ontology (GO)] terms and contain genes annotated by that term.</p>
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| − | <h2>C6: oncogenetic signatures</h2>
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| − | <p>Gene sets represent signatures of cellular pathways which are often dis-regulated in cancer. The majority of signatures were generated directly from microarray data from NCBI GEO or from in house unpublished expression profiling experiments which involved perturbation of known cancer genes. In addition, a small number of oncogenic signatures was curated from scientific publications.</p>
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| − | <h2>C7: immunologic signatures</h2>
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| − | <p>Gene sets that represent cell states and perturbations within the immune system. The signatures were generated by manual curation of published studies in human and mouse immunology. For each study, pairwise comparisons of relevant classes were made and genes ranked by mutual information. Gene sets correspond to top or bottom ranking genes (FDR < 0.25 or maximum of 200 genes) for each comparison. This resource is generated as part of the [http://www.immuneprofiling.org Human Immunology Project Consortium (HIPC)].</p>
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