Open HenrikBengtsson opened 4 years ago
$ for pkg in $pkgs; do echo "$pkg:"; (cd "$pkg"; grep -E "^[ \t]*[^#].*data[.]frame" -- */*.R | grep -vF stringsAsFactors;); echo; read -r -p "Press ENTER to continue ..."; done aroma.seq: R/agsub.R:agsub <- function(pattern, replacement, x, ..., default=NA_character_, as=c("matrix", "list", "data.frame")) { R/agsub.R: } else if (as == "data.frame") { R/BamDataFile.R: stats <- data.frame(length=seqLength, mapped=countMapped, unmapped=countUnmapped) R/BamDataFile.R: data <- as.data.frame(data) R/BwaIndexSet.R: if (length(idx) == 0) return(data.frame()) R/CnvKitCopyNumberRatioFile.R: data.frame(chromosome=chr, x=(data$start + data$end)/2, y=ploidy*2^data$log2, w=data$weight) R/countNucleotides.R: loci <- Arguments$getInstanceOf(loci, "data.frame") R/countNucleotides.R: loci <- Arguments$getInstanceOf(loci, "data.frame") R/GatkAlleleCounting.R: data <- data.frame(chromosome=chr, position=pos, counts) R/segmentByPairedPSCBS.SeqzFileSet.R: data <- data.frame( R/segmentByPairedPSCBS.SeqzFileSet.R:setMethodS3("binForPSCBS", "data.frame", function(data, binSize, ..., verbose=FALSE) { tests/agsub.R:for (as in c("list", "data.frame", "matrix")) { tests/countNucleotides.R:loci <- data.frame(chromosome=chrs[1L], pos=1:100) tests/countNucleotides.R:loci <- data.frame(chromosome=chrs, pos=1:100) tests/countNucleotides.R:loci <- data.frame(chromosome=chrs[1L], pos=1:100)