Add to ORKGThe ’COSMIC.67 ’ package provides the curated mutations published with the COSMIC release version 67 (2013-10-24). Both variants found in coding and non-coding regions are included and offered as (a) a single object of class ’CollapsedVCF ’ and (b) a bgzipped and tabix-index ’VCF’ file. Additionally, the package contains the cancer gene census, a list of genes causally linked to cancer. For details on the collection and curation of the original data, please see the webpage of the COS-MIC project
Abstract The Network of Cancer Genes (NCG) is a manually curated repository of 2372 genes whose soma...
Data files generated as part of a study into the influence of neighbouring bases on point mutation. ...
The zip file contains three folders, which group somatically acquired indels, structural variants an...
The genome sequence framework provided by the human genome project allows us to precisely map human ...
Figure S3. Cohort explorer for the whole TCGA LUAD cohort and our patient (1) Significant driver gen...
A. Distribution by type of mutation. The COSMIC mutations were partitioned into non-coding (5’ UTR, ...
"COSMIC, the Catalogue Of Somatic Mutations In Cancer":http://www.sanger.ac.uk/cosmic is d...
Mutations in hallmark genes are believed to be the main drivers of cancer progression. These mutatio...
<p>Coding mutations in known cancer genes (A) and candidate genes (B) are indicated with different c...
International audienceThe main databases devoted stricto sensu to cancer cytogenetics are the "Mitel...
Since 1989, about 570 different p53 mutations have been identified in more than 8000 human cancers. ...
Table S1. Significant mutually exclusive (ME) and co-occurring (CO) associations across all cancer t...
Supplementary methods and results. This document contains supplementary text about the multilevel ma...
<p>From the initial list of 461 genes amplified in one or more TCGA datasets, 73 amplified genes wer...
Mutations in hallmark genes are believed to be the main drivers of cancer progression. These mutatio...
Abstract The Network of Cancer Genes (NCG) is a manually curated repository of 2372 genes whose soma...
Data files generated as part of a study into the influence of neighbouring bases on point mutation. ...
The zip file contains three folders, which group somatically acquired indels, structural variants an...
The genome sequence framework provided by the human genome project allows us to precisely map human ...
Figure S3. Cohort explorer for the whole TCGA LUAD cohort and our patient (1) Significant driver gen...
A. Distribution by type of mutation. The COSMIC mutations were partitioned into non-coding (5’ UTR, ...
"COSMIC, the Catalogue Of Somatic Mutations In Cancer":http://www.sanger.ac.uk/cosmic is d...
Mutations in hallmark genes are believed to be the main drivers of cancer progression. These mutatio...
<p>Coding mutations in known cancer genes (A) and candidate genes (B) are indicated with different c...
International audienceThe main databases devoted stricto sensu to cancer cytogenetics are the "Mitel...
Since 1989, about 570 different p53 mutations have been identified in more than 8000 human cancers. ...
Table S1. Significant mutually exclusive (ME) and co-occurring (CO) associations across all cancer t...
Supplementary methods and results. This document contains supplementary text about the multilevel ma...
<p>From the initial list of 461 genes amplified in one or more TCGA datasets, 73 amplified genes wer...
Mutations in hallmark genes are believed to be the main drivers of cancer progression. These mutatio...
Abstract The Network of Cancer Genes (NCG) is a manually curated repository of 2372 genes whose soma...
Data files generated as part of a study into the influence of neighbouring bases on point mutation. ...
The zip file contains three folders, which group somatically acquired indels, structural variants an...