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gnomAD AF & family-based vcf analysis #34
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Hi @XiaKwan, Thanks for your patience. Regarding your questions,
Hope this helps. Best, |
Just curious, any update on trio-specific analysis using STAARpipeline? If you need an early tester using outside data, I would be happy to try it out. -Brian |
Hi @bmuchmore, Thank you very much for your interest! We are still developing methods for analyzing family data (trio design) using STAAR/STAARpipeline. We will let you know as soon as they are ready to be tested. Best, |
Hi Xihao,
Thanks for your useful tool! And I've met some problems really confused me:
I noticed that allele frequencies of gnomAD and 1000G are contained in FAVOR full database but not in FAVOR essential database. Are there any approaches that I could make use of these AF annotations in the STAAR procedure? (Like the variants with gnomAD AF < 5‰ will be given priority).
I'm now working on a rare disease and my cohort contains ~700 trio families (only the child has the disease, parents are healthy), so my data is a vcf file with ~2000 samples. Does STAAR pipeline support family-based analysis? If so, how can I represent this family relationship while analyzing? (maybe in the pheno.csv?)
Do I need to add more irrelevant healthy samples as control?
Thanks a lot!!!
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