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2.2 years ago
mathewarkit
•
0
Hi!
I have a doubt! Which bioinformatics analysis would you perform to prioritise disease driver variants from raw sequencing data? Along with computational methods, file formats, quality measures, controls, annotation and statistics to assign genomic disease?
I have been asked for it and I can't find any proper literature to answer it
Thanks!
map those raw sequencing data to a reference genome, extract the variants, filter the variants according to the studied disease.
I have no doubt. Just google "variant prioritization".
Thank you! I will google it right now!
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