fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

Whole Genome Sequencing analysis, WGS analysis

Identification & characterization of bacterial plasmid-borne contigs from short-read draft assemblies.

Rapid determination of appropriate reference genomes.

Call and score variants from WGS/WES of rare disease patients.

Snakemake-based workflow for detecting structural variants in genomic data

Analysis pipelines for genomic sequencing data

A tool to genotype CYP2D6 with WGS data

Data management of large-scale whole-genome sequence variant calls (Development version only)

Kourami: Graph-guided assembly for HLA alleles

Integrated copy number variation detection toolset

Workflow to construct linear representation of pan genome from deep WGS data and public assemblies

vSNP -- validate SNPs

Targeted Detection and Reconstruction of Plasmids

Exome/Capture/RNASeq Pipeline Implementation using snakemake

Bacterial analysis toolbox for full ESKAPE pathogen characterization and profiling the resistome, mobilome, virulome & phylogenomics using WGS

A NGS analysis framework for WGS data, which automates the entire process of spinning up AWS EC2 spot instances and processing FASTQ to snvVCF in <60m, for dollars a sample and achieving Fscores of 0.998.

Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores and annotations from popular disease databases. Seave stores genomic variation of all types and sizes, and allows filtering for specific inheritance patterns, quality values, allele frequencies and gene lists. …

经纬度转换，sqlldr入库，Geometry工具

PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)