Project Name | Stars | Downloads | Repos Using This | Packages Using This | Most Recent Commit | Total Releases | Latest Release | Open Issues | License | Language |
---|---|---|---|---|---|---|---|---|---|---|
Vg | 1,022 | 3 months ago | 760 | other | C++ | |||||
tools for working with genome variation graphs | ||||||||||
Nucleus | 675 | 2 | 3 years ago | 18 | August 31, 2021 | 1 | other | C++ | ||
Python and C++ code for reading and writing genomics data. | ||||||||||
Htsjdk | 271 | 170 | 87 | 4 months ago | 78 | October 13, 2023 | 303 | Java | ||
A Java API for high-throughput sequencing data (HTS) formats. | ||||||||||
Genomics | 154 | 2 years ago | 2 | R | ||||||
A collection of scripts and notes related to genomics and bioinformatics | ||||||||||
Cljam | 87 | 3 months ago | 37 | May 10, 2019 | 6 | apache-2.0 | Clojure | |||
A DNA Sequence Alignment/Map (SAM) library for Clojure | ||||||||||
Snps | 82 | 1 | 2 | 3 months ago | 42 | June 06, 2022 | 23 | bsd-3-clause | Python | |
tools for reading, writing, merging, and remapping SNPs | ||||||||||
Strangervisions | 35 | 7 years ago | 2 | gpl-3.0 | Python | |||||
Sccaller | 28 | a year ago | 3 | agpl-3.0 | Python | |||||
Single Cell Caller (SCcaller) - Identify single nucleotide variations (SNVs) from single cell sequencing data | ||||||||||
Germline Dna | 23 | a year ago | 2 | mit | wdl | |||||
A BioWDL variantcalling pipeline for germline DNA data. Starting with FASTQ files to produce VCF files. Category:Multi-Sample | ||||||||||
Genomic Data Science | 17 | 9 years ago | HTML | |||||||
Genomic data science specialization |