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+\name{mutCOM}
+\alias{mutCOM}
+\docType{data}
+\title{
+Genetic information of patient samples
+}
+\description{
+This \code{"\linkS4class{NChannelSet}"} object contains genetic data for samples investigated in any
+of the three experiments: whole exome sequencing, targeted sequencing or
+fluorescent in situ hybridization. Object consists of one channel called
+binary, with values: 0 if the mutation was absent, 1 if mutation was present
+or NA if the mutation was not investigated. Feature data of the object
+contains detailed information about mutation in TP53 and BRAF genes - the
+variant(s) detected ('*_CDS' and '*_AA' columns) and the percentage at which
+each variant was detected ('*_%' columns).
+For TP53, BRAF, KRAS, del17p13, UMODL1, CREBBP, PRPF8 and trisomy12 mutation
+an additional column 'cs' summarizes the clone size of
+the mutated population. This value is a fraction at which the most abundant
+variant is present in a sample.
+}
+\author{Małgorzata Oleś <dr.malgorzata.oles@gmail.com>}
+\usage{
+mutCOM
+}
+\format{
+\code{"\linkS4class{NChannelSet}"} object with 89 genes (columns) and 265 patient samples (rows).
+}
+\keyword{datasets}