cosmicGRCh37: COSMIC data mapped to GRCh37 (hg19)

Description Usage Format Details Source References Examples

Description

COSMIC data mapped to GRCh37 (hg19)

Usage

1

Format

The format is: Formal class 'GRanges' [package "GenomicRanges"] with 6 slots ..@ seqnames :Formal class 'Rle' [package "IRanges"] with 4 slots .. .. ..@ values : Factor w/ 24 levels "chr1","chr10",..: 2 4 15 18 4 18 12 8 21 9 ... .. .. ..@ lengths : int [1:11937] 2 13 3 1 6 3 2 2 2 1 ... .. .. ..@ elementMetadata: NULL .. .. ..@ metadata : list() ..@ ranges :Formal class 'IRanges' [package "IRanges"] with 6 slots .. .. ..@ start : int [1:65870] 52575931 52576024 9243930 9259164 9251272 9242564 9260237 9258837 9225356 9229975 ... .. .. ..@ width : int [1:65870] 1 1 1 1 1 1 1 1 1 1 ... .. .. ..@ NAMES : NULL .. .. ..@ elementType : chr "integer" .. .. ..@ elementMetadata: NULL .. .. ..@ metadata : list() ..@ strand :Formal class 'Rle' [package "IRanges"] with 4 slots .. .. ..@ values : Factor w/ 3 levels "+","-","*": 3 .. .. ..@ lengths : int 65870 .. .. ..@ elementMetadata: NULL .. .. ..@ metadata : list() ..@ elementMetadata:Formal class 'DataFrame' [package "IRanges"] with 6 slots .. .. ..@ rownames : NULL .. .. ..@ nrows : int 65870 .. .. ..@ listData :List of 24 .. .. .. ..$ Gene.name : Factor w/ 15198 levels "A1CF","A2M","A2ML1",..: 1 1 2 2 2 2 2 2 2 2 ... .. .. .. ..$ Accession.Number : Factor w/ 15158 levels "AB023190","AB051467.1",..: 9114 9114 10964 10964 10964 10964 10964 10964 10964 10964 ... .. .. .. ..$ HGNC.ID : int [1:65870] 24086 24086 7 7 7 7 7 7 7 7 ... .. .. .. ..$ Sample.name : Factor w/ 153739 levels " HOG06-122"," HOG06-1221",..: 118608 152091 111369 118525 128147 128152 128178 148952 148957 148996 ... .. .. .. ..$ ID_sample : int [1:65870] 1312984 1604872 1551882 1312971 1560554 1560559 1560588 1287214 1287216 1287244 ... .. .. .. ..$ ID_tumour : int [1:65870] 1223893 1524191 1473988 1223880 1482004 1482009 1482038 1198492 1198494 1198522 ... .. .. .. ..$ Primary.site : Factor w/ 43 levels "Fallopian tube",..: 8 33 33 8 40 40 40 8 8 8 ... .. .. .. ..$ Site.subtype : Factor w/ 172 levels "NS","abdomen",..: 16 44 1 16 70 70 96 16 16 16 ... .. .. .. ..$ Primary.histology : Factor w/ 84 levels "Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour",..: 40 23 57 40 23 23 23 40 40 40 ... .. .. .. ..$ Histology.subtype : Factor w/ 399 levels "ACTH","ACTH-FSH",..: 82 373 33 82 373 373 373 82 82 82 ... .. .. .. ..$ Genome.wide.screen : Factor w/ 3 levels "","n","y": 1 3 3 1 3 3 3 1 1 1 ... .. .. .. ..$ Mutation.ID : int [1:65870] 40879 138756 110440 39653 127216 127215 127217 35965 35963 35964 ... .. .. .. ..$ Mutation.CDS : Factor w/ 38881 levels "","Intronic",..: 38446 36685 14397 37309 9399 16660 34285 1522 22775 20223 ... .. .. .. ..$ Mutation.AA : Factor w/ 54163 levels "","p.","p.(1409)ins6",..: 9502 31055 16907 47270 51096 17136 53295 15450 11774 46083 ... .. .. .. ..$ Mutation.Description : Factor w/ 15 levels "Complex - compound substitution",..: 11 11 11 11 13 13 13 11 11 13 ... .. .. .. ..$ Mutation.zygosity : Factor w/ 3 levels "het","hom","unk": 1 3 2 1 3 3 3 1 1 1 ... .. .. .. ..$ Mutation.NCBI36.strand : Factor w/ 3 levels "","+","-": 3 1 1 3 1 1 1 3 3 3 ... .. .. .. ..$ Mutation.GRCh37.genome.position: Factor w/ 65871 levels "","10:100011329-100011329",..: 1305 1306 9761 9764 9762 9760 9765 9763 9757 9758 ... .. .. .. ..$ Mutation.GRCh37.strand : Factor w/ 3 levels "","+","-": 3 3 3 3 3 3 3 3 3 3 ... .. .. .. ..$ Mutation.somatic.status : Factor w/ 6 levels "Confirmed germline variant",..: 2 2 2 2 6 6 6 2 2 2 ... .. .. .. ..$ Pubmed_PMID : int [1:65870] 18772396 21984974 21499247 18772396 21798893 21798893 21798893 18772890 18772890 18772890 ... .. .. .. ..$ Sample.source : Factor w/ 27 levels "NS","autopsy - NOS",..: 23 23 24 23 24 24 24 24 24 24 ... .. .. .. ..$ Tumour.origin : Factor w/ 8 levels "NS","adenoma adjacent to primary tumour",..: 7 5 4 5 5 5 5 6 7 7 ... .. .. .. ..$ Comments : Factor w/ 2723 levels "","Age at tumour recurrence:1 year after diagnosis of TMD",..: 1002 1 1205 1002 1 1 1 1 1 1 ... .. .. ..@ elementType : chr "ANY" .. .. ..@ elementMetadata: NULL .. .. ..@ metadata : list() ..@ seqinfo :Formal class 'Seqinfo' [package "GenomicRanges"] with 4 slots .. .. ..@ seqnames : chr [1:24] "chr1" "chr10" "chr11" "chr12" ... .. .. ..@ seqlengths : int [1:24] NA NA NA NA NA NA NA NA NA NA ... .. .. ..@ is_circular: logi [1:24] NA NA NA NA NA NA ... .. .. ..@ genome : chr [1:24] NA NA NA NA ... ..@ metadata : list()

Details

The data are in a GRanges object with elementMetadata from the original download. Note that some of the ranges are large, so one may need to filter when looking for overlapping variants.

Source

ftp://ftp.sanger.ac.uk/pub/CGP/cosmic/data_export/CosmicMutantExport_v57_180112.tsv

References

http://www.sanger.ac.uk/genetics/CGP/cosmic/

Examples

1

seandavi/COSMIC.build57 documentation built on May 29, 2019, 4:28 p.m.