cnaPanTNBC: DNA CNV (germline) and CNA (tumor) data for TCGA samples
In sinnweja/panoply: Personalized Cancer Report
Description
Usage
Format
Examples
Description
Per-Gene DNA Copy Number Variation (germline) and Copy Number Alteration
(tumor) data for TCGA samples
Usage
1
data("cnaPanTNBC")
Format
A data frame with 77 subjects.
CHROMchromosome of gene
STARTgene start position
STOPgene stop position
geneidGene ID
Gene.Symbolgene symbol, NCBI
TCGA-A2-A04Tpatient identifier
Examples
1
2
sinnweja/panoply documentation built on Aug. 9, 2019, 9:56 a.m.
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Description Usage Format Examples
Description
Per-Gene DNA Copy Number Variation (germline) and Copy Number Alteration (tumor) data for TCGA samples
Usage
1 | data("cnaPanTNBC")
|
Format
A data frame with 77 subjects.
CHROMchromosome of gene
STARTgene start position
STOPgene stop position
geneidGene ID
Gene.Symbolgene symbol, NCBI
TCGA-A2-A04Tpatient identifier
Examples
1 2 |
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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