Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
-
Updated
Jul 26, 2026 - Nextflow
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Local-first, open-source Claude Science alternative, before Claude Science is a thing. Turn your AI agent into personal DNA expert.
Whole Genome Sequencing analysis, WGS analysis
A lightweight and handy variant calling pipeline generator for whole-genome sequencing (WGS) and whole exom sequencing data (WES) analysis by using GATK and Sentieon. 一个基于 GATK 和 Sentieon 的简易且全面的 WGS/WES 分析流程生成器.
Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data
An R package for performing STAAR procedure in whole-genome sequencing studies
vcfdist: Accurately benchmarking phased variant calls
An R package for performing association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using STAARpipeline
Detect novel (and reference) STR expansions from short-read data
MutMap pipeline to identify causative mutations responsible for a phenotype
QTL-seq pipeline to identify causative mutations responsible for a phenotype
Scalable SQLite database for fast querying of gnomAD variant annotations (allele frequency, depth, population metrics). Supports gnomAD v2-v4, WGS and WES.
mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data
PlasmidID is a mapping-based, assembly-assisted plasmid identification tool that analyzes and gives graphic solution for plasmid identification.
cfDNAPro specializes in standardized and robust cfDNA fragmentomic analysis
Assembly of Phylogenomic Datasets from High-Throughput Sequencing data
The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVORannotator, STAARpipeline and STAARpipelineSummary
A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification.
Clinical Whole Genome and Exome Sequencing Pipeline
Whole Exome/Whole Genome Sequencing alignment pipeline
Add a description, image, and links to the whole-genome-sequencing topic page so that developers can more easily learn about it.
To associate your repository with the whole-genome-sequencing topic, visit your repo's landing page and select "manage topics."