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| **Pigengene:** This R package provides an efficient way to perform network analysis and to infer biological signatures from gene expression profiles. The signatures are independent from the underlying platform, e.g., it can infer the signatures using data from microarray and evaluate them in an independent RNA Seq dataset. It is approved by, and publicly available from, [[https://bioconductor.org/packages/Pigengene|Bioconductor]]. | **Pigengene:** This R package provides an efficient way to perform network analysis and to infer biological signatures from gene expression profiles. The signatures are independent from the underlying platform, e.g., it can infer the signatures using data from microarray and evaluate them in an independent RNA Seq dataset. It is approved by, and publicly available from, [[https://bioconductor.org/packages/Pigengene|Bioconductor]]. |
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| **iNETgrate:** [[https://bitbucket.org/habilzare/genetwork/src/master/code/iNETgrate/|This]] R package is useful to integrate DNA methylation and gene expression data into //a single //network. This approach leads to identification of more robust gene modules compared to conventional coexpression networks. The package will be publicly available after review and approval by Bioconductor. | **iNETgrate:** This R package is useful to integrate DNA methylation and gene expression data into //a single //network [[[https://bitbucket.org/habilzare/genetwork/src/master/|code]]]. This approach leads to identification of more robust gene modules compared to conventional coexpression networks. The package will be publicly available after review and approval by Bioconductor. |
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| - 200 AML cases from TCGA (LAML dataset). Available data types include gene expression , DNA-methylation, CNV, mutation, etc. TCGA data moved to [[https://gdc-portal.nci.nih.gov/|GDC]] but DNA-methylation is not there. Instead, it can be retrieved from GDC Legacy Archive or the original [[https://tcga-data.nci.nih.gov/docs/publications/laml_2012/|paper]]. | - 200 AML cases from TCGA (LAML dataset). Available data types include gene expression , DNA-methylation, CNV, mutation, etc. TCGA data moved to [[https://gdc-portal.nci.nih.gov/|GDC]] but DNA-methylation is not there. Instead, it can be retrieved from GDC Legacy Archive or the original [[https://tcga-data.nci.nih.gov/docs/publications/laml_2012/|paper]]. |
| - German [[https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE37642|AMLCG]] 1999 provides microarray data of 562 AML samples. | - German [[https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE37642|AMLCG]] 1999 provides microarray data of 562 AML samples. |
| - Papaemmanuil, Elli, et al. "Genomic classification and prognosis in acute myeloid leukemia." [[http://www.nejm.org/doi/full/10.1056/NEJMoa1516192#t=article|NEJM]] 374.23 (2016): 2209-2221. \\ The mutations of 111 genes in over **1,500 AML** cases are reported. The authors used this information to classify cases into groups and showed these groups have different prognosis. I.,e., [[https://www.mskcc.org/sites/default/files/node/2246/documents/discrete-cpe.pdf|concordance]] (probability estimates) improves from 64% using only the European LeukemiaNet criteria to 71%. Using the alternative allele frequency, they estimated the time of occurrence for the driver mutations. The data are available through the links in the corresponding [[http://www.nature.com/ng/journal/v49/n3/full/ng.3756.html|Nature]] paper [[[:ng.3756.pdf?media=ng.3756.pdf|pdf]]]. Information on downloading these data is contained in the readme file found in genetwork:~/proj/genetwork/data/AML/gerstung/readme.txt. In particular, we have access to [[https://www.ebi.ac.uk/ega/studies/EGAS00001000275|EGAS00001000275]] through [[https://ega-archive.org/|EGA]] Archives. See [[:habils_lab_notebook|Habil's]] note on 2017/09/05 for more detail. Any member of Oncinfo Lab who touches (analyzes or views) these data from Sanger Institute must read and abide to the [[:sanger_data_agreement_2017-08-09.pdf?media=sanger_data_agreement_2017-08-09.pdf|agreement]]. | - Papaemmanuil, Elli, et al. "Genomic classification and prognosis in acute myeloid leukemia." [[http://www.nejm.org/doi/full/10.1056/NEJMoa1516192#t=article|NEJM]] 374.23 (2016): 2209-2221. \\ The mutations of 111 genes in over **1,500 AML** cases are reported. The authors used this information to classify cases into groups and showed these groups have different prognosis. I.,e., [[https://www.mskcc.org/sites/default/files/node/2246/documents/discrete-cpe.pdf|concordance]] (probability estimates) improves from 64% using only the European LeukemiaNet criteria to 71%. Using the alternative allele frequency, they estimated the time of occurrence for the driver mutations. The data are available through the links in the corresponding [[http://www.nature.com/ng/journal/v49/n3/full/ng.3756.html|Nature]] paper [[:ng.3756.pdf?media=ng.3756.pdf|pdf]]]. Information on downloading these data is contained in the readme file found in genetwork:~/proj/genetwork/data/AML/gerstung/readme.txt. In particular, we have access to [[https://www.ebi.ac.uk/ega/studies/EGAS00001000275|EGAS00001000275]] through [[https://ega-archive.org/|EGA]] Archives. See [[:habils_lab_notebook|Habil's]] note on 2017/09/05 for more detail. Any member of Oncinfo Lab who touches (analyzes or views) these data from Sanger Institute must read and abide to the [[:sanger_data_agreement_2017-08-09.pdf?media=sanger_data_agreement_2017-08-09.pdf|agreement]]. |
| - RNA, DNA methylation, whole genome, etc. data of 960 (pediatric?) AML cases are available from [[https://ocg.cancer.gov/programs/target/acute-myeloid-leukemia|TARGET]] AML study. | - RNA, DNA methylation, whole genome, etc. data of 960 (pediatric?) AML cases are available from [[https://ocg.cancer.gov/programs/target/acute-myeloid-leukemia|TARGET]] AML study. |
| - AML-NK gene expression data (RNA-Seq) from three datasets (TCGA, Leucegene, and PMP/BCCA). [[https://docs.google.com/a/princeton.edu/document/d/1tB75BDAoG6-ggkoKzxF_f8anTnaP0lOAZ4MG-wEWCyk/edit?usp=sharing|Full description]]. | - AML-NK gene expression data (RNA-Seq) from three datasets (TCGA, Leucegene, and PMP/BCCA). [[https://docs.google.com/a/princeton.edu/document/d/1tB75BDAoG6-ggkoKzxF_f8anTnaP0lOAZ4MG-wEWCyk/edit?usp=sharing|Full description]]. |
| - Genomic Data Commons ([[https://portal.gdc.cancer.gov/repository|GDC]]), which contains TCGA data and more. | - Genomic Data Commons ([[https://portal.gdc.cancer.gov/repository|GDC]]), which contains TCGA data and more. |
| - [[https://amp.pharm.mssm.edu/archs4/|ARCHS4]], which was developed at the Icahn School of Medicine at Mount Sinai, and provides tools to download and analyze RNA-Seq data including single-cell gene expression. | - [[https://amp.pharm.mssm.edu/archs4/|ARCHS4]], which was developed at the Icahn School of Medicine at Mount Sinai, and provides tools to download and analyze RNA-Seq data including single-cell gene expression. |
| | - The [[https://www.nature.com/articles/s41586-018-0623-z#Sec38|BEAT]] ALM dataset of ~300 cases including gene expression, survival, ELN17, etc. |
| | - [[https://www.leukemiaatlas.org/adultaml|Leukemia Protein Atlas]]: Expression of hundreds of proteins were measured in bone marrow and PB samples of ~200 AML cases. A good publicly available resource to validate findings based on gene expression assays. |
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| ===== Related work ===== | ===== Related work ===== |
