Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms

Breakpoints via assembly - Identifies breaks and attempts to assemble rearrangements in whole genome sequencing data.

GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS

Explore and filter structural variant calls from Lumpy and Delly VCF files

Custom options for using k2pdfopt to convert papers and pdf books to kindle compatible PDFs