GPF: Genotypes and Phenotypes in Families
-
Updated
May 20, 2024 - Python
GPF: Genotypes and Phenotypes in Families
Open-source feature management solution built for developers.
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
Step into my world of code and creativity, where pixels come alive and ideas turn into digital realities. I'm thrilled to have you here, exploring my projects, skills, and passion for technology.
Croatian Chess is a collection of various chess variants, starting as a simple and natural enhancement to classical chess and growing ever more complex with each new variant.
Structural variation and indel detection by local assembly
Protegenomics analysis based on Pangenome references
GO Feature Flag is a simple, complete and lightweight self-hosted feature flag solution 100% Open Source. 🎛️
🧬 Cancer research, simulations and science.
WebApp for DNA variants interpretation
Data created for www.STEPBible.org, available to other projects under CC BY 4.0
SEARCH V4 :: The aim of the project is to integrate ClinGen's internal data services and public external data services around a common user experience to ensure clinically relevant knowledge about genes and variants is available for use in precision medicine and research.
GDBIGtools: A command line tools for GDBIG varaints browser
CIViC is an open access, open source, community-driven web resource for Clinical Interpretation of Variants in Cancer
Command line tools for CMDB varaints browser
🦄 Tailwindcss first-class variant API
Small variant, structural variant, and short tandem repeat phasing tool for PacBio HiFi reads
Easily abstract and compose your React Tailwind classes
A Tool to Annotate and Prioritize Exome Variants
Add a description, image, and links to the variants topic page so that developers can more easily learn about it.
To associate your repository with the variants topic, visit your repo's landing page and select "manage topics."