Detection of CNVs (deletion/duplication) in target panel based NGS data

The official Python library for the OpenAI API

Open source code for AlphaFold 2.

structural variant database software

Support Vector Structural Variation Genotyper

Structural variant and indel caller for mapped sequencing data

A structural variation pipeline for short-read sequencing

Invoke is a leading creative engine for Stable Diffusion models, empowering professionals, artists, and enthusiasts to generate and create visual media using the latest AI-driven technologies. The …

DELLY2: Structural variant discovery by integrated paired-end and split-read analysis

TIDDIT - structural variant calling

a python extension of CNVnator -- a tool for CNV analysis from depth-of-coverage by mapped reads

Markdown Cheatsheet for Github Readme.md

Haplotype VCF comparison tools

Repository for the CWL standards. Use https://cwl.discourse.group/ for support 😊