JasonAHendry's Stars
torvalds/linux
Linux kernel source tree
gabime/spdlog
Fast C++ logging library.
facebookresearch/hydra
Hydra is a framework for elegantly configuring complex applications
filipdutescu/modern-cpp-template
A template for modern C++ projects using CMake, Clang-Format, CI, unit testing and more, with support for downstream inclusion.
lh3/seqtk
Toolkit for processing sequences in FASTA/Q formats
arq5x/bedtools2
bedtools - the swiss army knife for genome arithmetic
kigster/cmake-project-template
This project is aimed at jump-starting a C/C++ project that can build libraries, binaries and have a working unit test suite. It uses CMake build system and is deliberately completely minimal.
antfu/iroiro
Beautiful Colors Lookup in CLI
nanoporetech/dorado
Oxford Nanopore's Basecaller
benjjneb/dada2
Accurate sample inference from amplicon data with single nucleotide resolution
dellytools/delly
DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
bactopia/bactopia
A flexible pipeline for complete analysis of bacterial genomes
whatshap/whatshap
Read-based phasing of genomic variants, also called haplotype assembly
mbhall88/rasusa
Randomly subsample sequencing reads or alignments
EBI-Metagenomics/emg-viral-pipeline
VIRify: detection of phages and eukaryotic viruses from metagenomic and metatranscriptomic assemblies
esteinig/nanoq
Minimal but speedy quality control for nanopore reads in Rust :bear:
wrpearson/fasta36
Git repository for FASTA36 sequence comparison software
genome/breakdancer
SV detection from paired end reads mapping
twolinin/longphase
gear-genomics/tracy
Basecalling, alignment, assembly and deconvolution of Sanger Chromatogram trace files
helske/seqHMM
Multivariate and Multichannel Discrete Hidden Markov Models for Categorical Sequences
TuringLang/AbstractMCMC.jl
Abstract types and interfaces for Markov chain Monte Carlo methods
odelaneau/shapeit5
Segmented HAPlotype Estimation and Imputation Tool
vplagnol/ExomeDepth
ExomeDepth R package for the detection of copy number variants in exomes and gene panels using high throughput DNA sequencing data.
at-cg/minichain
Long-read aligner to pangenome graphs
stuckyb/seqtrace
User-friendly software for viewing and processing Sanger DNA sequencing trace files.
malariagen/pipelines
Pipelines for processing malaria parasite and mosquito genome sequence data.
Genomicsplc/wecall
Fast, accurate and simple to use command line tool for variant detection in NGS data.
iTaxoTools/Hapsolutely
Reconstruct haplotypes and produce genealogy graphs from population data
altairwei/bioutils
C++ Library written to solve the ROSALIND problems