TCGA_A8_A0A7_maf: SNVsReadCountsFile for sample TCGA-A8-A0A7
In TPES: Tumor Purity Estimation using SNVs
Description
A data frame object containing the read counts data of somatic
single nucleotide variants (SNVs) loci for sample TCGA-A8-A0A7.
The header contains the chromosme that harbors the SNV ("chr" column),
the position of the SNV (defined by the "start" and "end" columns),
the informations about the reference and alternative base counts ("ref.count"
and "alt.count" columns, respectively) and finally the sample ID ("sample"
column). For more information please visit
MAF file format.
Format
A data.frame object.
TPES documentation built on May 2, 2019, 1:44 p.m.
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Description
A data frame object containing the read counts data of somatic single nucleotide variants (SNVs) loci for sample TCGA-A8-A0A7. The header contains the chromosme that harbors the SNV ("chr" column), the position of the SNV (defined by the "start" and "end" columns), the informations about the reference and alternative base counts ("ref.count" and "alt.count" columns, respectively) and finally the sample ID ("sample" column). For more information please visit MAF file format.
Format
A data.frame object.
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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