How is Mutation.Count derived in TCGA?
Hi!
TCGA provides a Mutation.Count value per patient. I couldn't find out how it was derived. It ranges from 8-158 for the different patients. Any suggestions where I can find clarification?
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can you show us where you found it, which context? which tumor?
it sounds to me that that's simply the count of mutations per patient
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Hi,
Of course, for example in this HGSOC patient:
Please use
ADD REPLY/ADD COMMENTwhen responding to existing posts to keep threads logically organized.that's the total # of mutations in the patient. you can easily check it on cBioportal http://www.cbioportal.org/case.do?cancer_study_id=ov_tcga&case_id=TCGA-04-1331
ps. as genomax2 mentioned, if you could move this below my answer that would help keeping this tidy and in logical order :)
I also ask my self this question.. what is the meaning of mutation.count? are we talking about all mutations or only non-synonymous? does this relate only to gene regions or whole genome mutations?