abrahamdsl/just_another_variant_calling_pipeline
Variant Calling Pipeline, just another one.
This is a program to map variances that were retrieved on a created, mostly similar genome, to the origin/base genome. Takes in variances (SNPs and INDELs only for now) in VCF format, gets its nearby X sequences to the left and right and these are BLAST-ed into the original genome. Best hit is selcted and the sequence is reduced again to to infer the location in new genome.
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Variant Calling Pipeline, just another one.
Automatically exported from code.google.com/p/the-uplb-express-ticketing-system
A set of scripts to gather data from //github.com/edgedalmacio/phisix
Converts an internal feature format representation to GFF3