CDP Genome Analysis Pipeline
Scripts and workflows for processing whole-genome sequencing (WGS) data from
Constitutional Delayed Puberty (CDP) samples — from raw sequencing reads
through joint-called variant files and downstream statistical analyses.
Overview
This repository contains the complete bioinformatics pipeline used to:
- Process raw WGS data (FASTQ → aligned BAM)
- Call structural variants (SVs), short tandem repeats (STRs), and small
variants (SNVs/indels) per s
This is a companion discussion topic for the original entry at github.com/xuefzhao/cdp-genome-analysis/InferIntervalList