############################################################
#
# author: Ludwig Geistlinger
# date: 2022-07-13 15:24:52
#
# descr: construction of HEK293T_HCT116_exon_counts
# DEXSeqDataSet from GEO
#
############################################################
# RNA-seq data for HEK293T cells was obtained from GEO accession GSE122633
# (runs labeled UnTfx1, UnTfx2 and UnTfx3 were used as those assayed untransformed
# wild type HEK293T cells)
# RNA-seq data for HCT116 cells was obtained from GEO accession GSE52429
# (runs labeled repPF and repPJ were used as those assayed untransformed wild type
# HCT116 cells)
# The reads were aligned to the GRCh38.104 genome by STAR 2.7.9a
# and counted by DEXseq 1.42.0.
# The resulting DEXSeqDataSet was filtered to exclude genes for which all exons
# have zero read counts using the following code:
# ("dxd" is the name of the DEXSeqDataSet)
library(DEXSeq)
rs <- rowSums(assay(dxd)[,1:5])
all.zero <- unname(rs) == 0
spl <- split(all.zero, rowData(dxd)$groupID)
all.zero <- vapply(spl, all, logical(1))
all.zero <- names(spl)[all.zero]
ind <- rowData(dxd)$groupID %in% all.zero
dxd <- dxd[!ind,]
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