Comments (8)
Yeah, the list of genes that are target for predisposition screening was simply a choice I made. The previous configuration was a bit too messy to handle. Either way, I'd be happy to create the specific gene set you are using as an additional virtual panel (aka UMCCR track:-))
Regarding ploidy and purity you are correct; these are not used in any way other than for display right now (I have no big clue as to how they could be used for filtering, as the purity and ploidy preferably should be taken into account when considering the variant set that is fed as input.
Wrt tumor type I believe I should add the option of not specifying any type, the 'Cancer_Unknown_Primary_NOS' is in fact a distinct cancer subtype, and should not be confused with not having specified a type at all. Sorry for not considering this.
Best,
Sigve
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Attaching an example VCF with such variant:
CHEK2.vcf.gz
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Hi Vlad,
Check out the new release, should place variants with conflicting interpretations of pathogenicity (from ClinVar) in the tier 3 table.
cheers,
Sigve
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Wow, thanks so much for the release, Sigve! That's highly anticipated. Will give it it run
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Cool. Happy bug-hunting :D
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Had to adapt for the command line options, but otherwise no bugs noticed :)
One thing is that you removed the predisposition gene list from the toml. Currently we pre-subset the germline variants to our own gene list (which is a combination of your list and CancerGeneCensus germline) before feeding them into CPSR, so in a way wanted to avoid additional hard-filtering. Though that's not critical I think given that overall improvements are so significant.
Also check out the updates to PCGR as well. Nice that it reports purity and ploidy, I will take them from PURPLE caller that we use for CN calling. But curious if purity/ploidy are used only to show in the report, or also for filtering somehow?
Also you made tumor_type
required now, but we don't yet specify it in our pipeline on a regular basis. I will just set it to Cancer_Unknown_Primary_NOS
, do you think it is fine for a general case? A lot of our tumors are CUPs anyway and that's why we don't even parameterize our analysis by tumor type.
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And thanks for parametrizing vep_pick_order
:)
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Cool. Would be really awesome to have the option of generic cancer type!
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Related Issues (20)
- Failed to instantiate plug in LoF HOT 3
- Custom panel HOT 11
- ERROR while running HOT 3
- cpsr_validate_input.py: error: argument vcf_validation: invalid int value: '/home/zdjzyx01/biosoft/cpsr/cpsr.toml' HOT 11
- Missed variant due to transcript pick? HOT 9
- cpsr_configuration_default.toml missing from PCGR data HOT 2
- Error: Problem with `mutate()` input `ACMG_PVS1_1`. HOT 4
- Error in loadNamespace(name) : there is no package called 'reactable' HOT 2
- x object 'GWAS_CITATION' not found HOT 3
- ImportError: No module named toml HOT 1
- minor typo in src/cpsr_functions.R HOT 1
- Error: `x` and `y` must share the same src HOT 5
- genes being excluded from CPSR exploratory track HOT 5
- Not able to download the data bundles (404 Error) HOT 2
- ACMG guideline updated to version 3.0. New genes were added to the secondary finding gene list. HOT 2
- make infromation like ckb to cpsr HOT 4
- Encounter the error in cpsr-report-generation() HOT 3
- Installation Instructions Only Describe Conda HOT 2
- Add sif file for running on an HPC HOT 1
- Biomarker variants not in Pathogenic/Likely Pathogenic section of report HOT 1
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