TCGA_HT_8564_maf: SNVsReadCountsFile for sample TCGA-HT-8564

Description Format


A data frame object containing the read counts data of somatic single nucleotide variants (SNVs) loci for sample TCGA-HT-8564. 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.


A data.frame object.

TPES documentation built on Jan. 12, 2019, 1:05 a.m.