A simple neural network for calling het-/hom-variants from alignments of single molecule reads to a reference

Toolkit for analyzing genetics data from admixed populations

A massively parallel, high-level programming language

A simple way to calibrate your neural network.

A Set of R Tools for Splitting up Chromosomes into Regions of High and Low Recombination

Frequently used commands in Bioinformatics

GRUD is a genotype imputation based on deep learning algorithms

Split Transformer Impute source code

CUDA-based KING relatedness estimation

The Book of Statistical Proofs

Smart and Accurate Polishing of Phase Haplotypes Integrating Read Enhancements (SAPPHIRE)

🌿 🍞 Large scale ancestry inference from PCA data

Github Pages template for academic personal websites, forked from mmistakes/minimal-mistakes

Script used to identify de novo variants from sequencing data.

Carbon Language's main repository: documents, design, implementation, and related tools. (NOTE: Carbon Language is experimental; see README)

Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls