PaCBAM: fast and scalable processing of whole exome and targeted sequencing data.

Samuel ValentiniTarcisio FedrizziFrancesca DemichelisAlessandro Romanel

Published in: BMC genomics (2019)

PaCBAM is a fast and scalable tool designed to process genomic regions from NGS data files and generate coverage and pileup comprehensive statistics for downstream analysis. The tool can be easily integrated in NGS processing pipelines and is available from Bitbucket and Docker/Singularity hubs.

Keyphrases

electronic health record
big data
copy number
single cell
healthcare
artificial intelligence
dna methylation
drug delivery
genome wide