Stars
Extensible specification for representing and uniquely identifying biological sequence variation
Open Source Qualtrics Alternative
Learning materials for the 3000788 Introduction to Computational Molecular Biology course
🍪 SEnsible Step-wise Analysis of DNA MEthylation BeadChips
A privacy-first, open-source platform for knowledge management and collaboration. Download link: http://github.com/logseq/logseq/releases. roadmap: https://logseq.io/p/NX4mc_ggEV
Personal CRM. Remember everything about your friends, family and business relationships.
10 Weeks, 20 Lessons, Data Science for All!
🃏 A magical documentation site generator.
minimizer-space de Bruijn graphs (mdBG) for whole genome assembly
Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling
Clair: Exploring the limit of using deep neural network on pileup data for germline variant calling
an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.
The open source embeddable online markdown editor (component).
The FASTEST QUALITY hash function, random number generators (PRNG) and hash map.
CNVar: an accurate knowledge-based copy number variation detection tool by maximum likelihood
Simple forum software for building great communities.
A software package for calculating, applying, evaluating and plotting the results of polygenic risk scores
A pandoc LaTeX template to convert markdown files to PDF or LaTeX.
Clairvoyante: a multi-task convolutional deep neural network for variant calling in Single Molecule Sequencing
Book about interpretable machine learning