Analysis of human whole genome sequencing (WGS) data using PacBio long-read sequencing data. This workflow uses raw PacBio FASTQ data from specified affected and unaffected persons, and produces read alignments, phased variant calls, gVCF files, and structural variant (SV) signatures for each individual.
smrtcells_sample_trial.cohort_info: An object containing two array-type keys,
unaffected_persons, each of which is s
This is a companion discussion topic for the original entry at github.com/DNAstack/PacBio-Workflows/Pacbio-Human-WGS-Workflow