SVs, noncoding mutations for CCLE data

in studies generating new gene models like this one Aberrant splicing isoforms detected by full-length transcriptome sequencing as transcripts of potential neoantigens in non-small cell lung cancer | Genome Biology | Full Text (biomedcentral.com)

We may need non-coding variants to analyze neoantigens. I am wondering is it possible to provide the vcf file or some more variants, which will be very helpful for researchers. Otherwise we need to run the variant call locally, which can be much more challenging.

The files can be gzipped which will greatly reduce the file sizes and save the bandwidth.
Thank you!

Hi,

Thanks for reaching out. In fact we do provide unfiltered mutect2 VCFs through our Terra workspace under the column name ā€œmutect2_vcf_wgsā€. Please see this post for details on how to access this data.

Thanks,
Simone

1 Like