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ClairS-TO - a deep-learning method for tumor-only somatic variant calling
✂️ ⚡ Rapid haploid variant calling and core genome alignment
software tools for haplotype assembly from sequence data
A fast, scalable, and accurate local ancestry method.
Fast and accurate in silico inference of HLA genotypes from RNA-seq
Microsatellite Instability (MSI) detection using high-throughput sequencing data.
microsatellite instability detection using tumor only or paired tumor-normal data
HiC for copy Number variation and Translocation detection
Deep learning based processing of Atac-seq data
Use Garry Tan's exact Claude Code setup: 23 opinionated tools that serve as CEO, Designer, Eng Manager, Release Manager, Doc Engineer, and QA
TypeScript is a superset of JavaScript that compiles to clean JavaScript output.
😸 Soothing pastel theme for the high-spirited!
Tools for plotting methylation data in various ways
A library for converting HTML into PDFs using ReportLab
trackc aims to produce beautiful genome tracks that are highly customizable
“When everything is connected to everything else, for better or worse, everything matters.” Bruce Mau
Jupyter notebook based genomic data visualization toolkit.
The awesome collection of OpenClaw skills. 5,400+ skills filtered and categorized from the official OpenClaw Skills Registry.🦞
A curated list of awesome Claude Skills, resources, and tools for customizing Claude AI workflows
The largest open-source medical AI skills library for OpenClaw🦞.
gghic makes visualization of Hi-C/-like data easily in R
Fast alignment and preprocessing of chromatin profiles