RNAseq.fpkms | R Documentation |
Genome-wide substitute reads with fragments per kilobase of exon per million reads mapped (FPKM) for the 15 cell lines specified in CL.subset
, derived from a comprehensive
collection of RNAseq profiles described in [1] and used in [2] to assess CRISPRcleaneR results.
data(RNAseq.fpkms)
A data frame with one bservations per gene and one variable per cell line. Row names indicates HGNC symbols and column names indicate cell line COSMIC identifiers [3].
[1] Garcia-Alonso L, Iorio F, Matchan A, et al. Transcription factor activities enhance markers of drug response in cancer doi: https://doi.org/10.1101/129478
[2] Iorio, F., Behan, F. M., Goncalves, E., Beaver, C., Ansari, R., Pooley, R., et al. (n.d.). Unsupervised correction of gene-independent cell responses to CRISPR-Cas9 targeting.
http://doi.org/10.1101/228189
[3] Forbes SA, Beare D, Boutselakis H, et al. COSMIC: somatic cancer genetics at high-resolution
Nucleic Acids Research, Volume 45, Issue D1, 4 January 2017, Pages D777-D783,
CL.subset
data(RNAseq.fpkms)
head(RNAseq.fpkms)
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