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## Data Request: Complete Mutation Information of BBC Patients
**Request Background:**
I recently came across your research study titled "Evolution of synchronous female bilateral breast cancers …
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- [x] Methylation tab cBioPortal/cbioportal#7683
- [ ] Should we support continuous CNA data?
- [x] Support patient level enrichments analysis cBioPortal/cbioportal#4637
- [x] treat overlapping pa…
jjgao updated
6 months ago
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Maybe this is just a future phase of generic assay implementation that we haven't gotten to yet, but generic assay data isn't visible anywhere on the patient/sample pages. Let's add it!
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Hello! I find this tool incredibly useful. Just one possible enhancement could be to report the upstream and downstream bases (context) of the mutation to make it easier to make mutational signatures …
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Hello,
I am trying SUITOR to extract signatures from cancer mutational catalogs. However, the "rec" object that is created after running the suitor() function, does not have any information on the W …
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Hi there!
I've been interested in estimating the contribution of mutational signatures defined originally with whole-genome data to variant calls from panels such as MSK-IMPACT ; I wonder what the…
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Can you please curate this study?
http://www.nature.com/ng/journal/v48/n10/full/ng.3659.html
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The idea is to build a classification algorithm for languages based on the frequency of occurence of a given charfacter set. These would work similar than mutational signatures.
The idea is to downlo…
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Most of analysis require resources or files such as reference genomes, mutational signatures in human cancer,... that are independent of your input data. These files can be big and they should not be …
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Hi,
I have been exploring the package and so far it has been very useful (specially since it is my first time working with mutational signatures). I generated the freq/Count of a number of selecte…