CELLector.CellLinesVarCatalog | R Documentation |
List of somatic variants found in cell-lines, from Iorio et al, Cell 2016 [1]
data("CELLector.CellLinesVarCatalog")
A data frame with 486243 observations (one for each somatic variants) on the following 13 variables.
SAMPLE
a character vector specifying the name of the cell line in which the variant has been found
COSMIC_ID
a numeric vector specifying COSMIC [2] identifier of the cell line in which the variant has been found
Cancer.Type
a character vector specifying the TCGA [3] classification of the tissue of origin of the cell line in which the variant has been found
Gene
a character vector specifying the HUGO [4] symbol of the gene hosting the variant under consideration (from Ensemble v56)
Transcript
a character vector specifying the identifier of the transcript affected by the variant under consideration (from Ensemble v56)
cDNA
a character vector specifying variant position and nucleotide change relating to the cDNA
AA
a character vector specifying aminoacid positon and alteration related to the variant under consideration
Classification
a character vector specifying a summary of the variant type (e.g. missense, frameshift, nonsense, etc)
Gene_list
a character vector: when non empty then the variant is within a high-confidence cancer driver gene (according to [1]), thus resulting in a cancer functional event (CFE) summarised in the Cell line Binary Event Matrices (BEMs)
Recurrence.Filter
a character vector: if 'Yes' then the variant under consideration is observed in COSMIC [2] (v68) at a minimal threshold frequency (specified in [1])
Subs
a numeric vector: Missense/substitution variants occurring in codons mutated in the systematic screen data in COSMIC [2] (v68) (select >=3
Truncating
a numeric vector: Truncating variant count from the systematic screen data in COSMIC [2] (v68) (select >10)
inframe
a numeric vector: Inframe indel alterations occurring in codons mutated in the systematic screen data in COSMIC [2] (v68) (select >=3)
Francesco Iorio (fi9323@gmail.com)
[1] Iorio, F. et al. A Landscape of Pharmacogenomic Interactions in Cancer. Cell 166, 740–754 (2016).
[2] Forbes, S. A. et al. COSMIC: exploring the world’s knowledge of somatic mutations in human cancer. Nucleic Acids Res. 43, D805–11 (2015).
[3] Hutter C and Zenklusen JC. The Cancer Genome Atlas: Creating Lasting Value beyond Its Data. Cell. 2018;173(2):283–285. doi:10.1016/j.cell.2018.03.042
[4] Braschi, B. et al. Genenames.org: the HGNC and VGNC resources in 2019. Nucleic Acids Res. Epub 2018 Oct 10. PMID: 30304474 DOI: 10.1093/nar/gky930
CELLector.CellLine.BEMs
, CELLector.CellLine.BEMs_v2
, CELLector.CFEs
data(CELLector.CellLinesVarCatalog) head(CELLector.CellLinesVarCatalog)
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