eddy-tb's Stars
torvalds/linux
Linux kernel source tree
twitter/the-algorithm
Source code for Twitter's Recommendation Algorithm
Cyan4973/xxHash
Extremely fast non-cryptographic hash algorithm
alexdobin/STAR
RNA-seq aligner
broadinstitute/gatk
Official code repository for GATK versions 4 and up
VerbalExpressions/PythonVerbalExpressions
Python regular expressions made easy
Martinsos/edlib
Lightweight, super fast C/C++ (& Python) library for sequence alignment using edit (Levenshtein) distance.
kangtegong/self-learning-cs
『혼자 공부하는 컴퓨터구조 & 운영체제』 (한빛미디어)
mummer4/mummer
Mummer alignment tool
whatshap/whatshap
Read-based phasing of genomic variants, also called haplotype assembly
brentp/smoove
structural variant calling and genotyping with existing tools, but, smoothly.
ryanlayer/giggle
Interval data structure
vibansal/HapCUT2
software tools for haplotype assembly from sequence data
woowabros/nestjs-library-crud
Automatically generate CRUD Rest API based on NestJS and TypeOrm
Illumina/ExpansionHunter
A tool for estimating repeat sizes
brentp/peddy
genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF
nhansen/SVanalyzer
Tools for the analysis of structural variation in genomes
ryanlayer/stix
Structural Variant Index
mcfrith/last-genome-alignments
fritzsedlazeck/parliament2
Runs a combination of tools to generate structural variant calls on whole-genome sequencing data
Jiefei-Wang/Painless-R-compilation-and-installation-on-Ubuntu
recipe for all dependencies of R on Ubuntu
mquinodo/AutoMap
Tool to find regions of homozygosity (ROHs) from sequencing data.
skandlab/SMuRF
Illumina/RepeatCatalogs
dpuiu/MitoHPC
brentp/svtyper
Bayesian genotyper for structural variants
UCSantaCruzComputationalGenomicsLab/last
Copy of the last aligner
brentp/longSTR
Call STRs in long reads or assembled contigs using TRF
brentp/svpack
Structural variant (SV) analysis tools
brentp/svtools
Tools for processing and analyzing structural variants.