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Planned Analysis: Oncoprint showing landscape of genetic lesions across PBTA. #6
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I imagine this analysis would make use of consensus SNV calls (#30), consensus CNV calls (#128), and filtered/prioritized fusion calls (#39 and #10) currently tied to multiple PRs. I can work on this after a grant submission Nov 15, but if anyone would like to work on this earlier, I have created some code for this for a recent manuscript that can be adapted. |
I can begin working on this issue now, while keeping in mind that this analysis will need to be rerun once the aforementioned upstream issues are completed. |
Thanks, @cbethell ! |
The code in
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Closing all planned analysis tickets in favor of opening new proposed analysis/updated analysis tickets as needed. |
This figure typically focuses on a set of high frequency and cancer associated lesions (mutations / CNV) and will typically have corresponding phenotypic data so as to visualize associations. See Figure 1 (https://www.biorxiv.org/content/10.1101/656587v1.full) for an example.
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