Hello,
I was working with this dataset
When I read the publication I understood they had RNA-seq data but in cBio portal is not avaiable.
"Transcriptome libraries were prepared using 200–1,000 ng of total RNA.
PolyA+ RNA isolation, cDNA synthesis, end-repair, A-base addition, and ligation
of the Illumina indexed adapters were performed according to the TruSeq
RNA protocol (Illumina). Libraries were size selected for 250–300 bp cDNA
fragments on a 3% Nusieve 3:1 (Lonza) gel, recovered using QIAEX II reagents
(QIAGEN), and PCR amplified using Phusion DNA polymerase (New England
Biolabs). Total transcriptome libraries were prepared as above, omitting the
poly A selection step and captured using Agilent SureSelect Human All Exon
V4 reagents and protocols. Library quality was measured on an Agilent 2100
Bioanalyzer for product size and concentration. Paired-end libraries were
sequenced with the Illumina HiSeq 2500, (23100 nucleotide read length)
with sequence coverage to 50 M paired reads and 100 M total reads.
Paired-end transcriptome sequencing reads were aligned to the human
reference genome (GRCh37/hg19) using a RNA-seq spliced read mapper
Tophat2 (Kim and Salzberg, 2011) (Tophat 2.0.4), with ‘‘–fusion-search’’ option
turned on to detect potential gene fusion transcripts. Potential false-positive
fusion candidates were filtered out using ‘‘Tophat-Post-Fusion’’ module.
Further, the fusion candidates were manually examined for annotation and
ligation artifacts. Gene expression, as fragments per kilobase of exon per
million fragments mapped (FPKM; normalized measure of gene expression),
was calculated using Cufflinks"
Are you going to add this new data in the new update or before?
Regards
Alberto