| vgteam/vg |
1,022 |
|
0 |
0 |
about 2 years ago |
0 |
|
760 |
other |
C++ |
| tools for working with genome variation graphs |
| google/nucleus |
675 |
|
0 |
2 |
over 4 years ago |
18 |
August 31, 2021 |
1 |
other |
C++ |
| Python and C++ code for reading and writing genomics data. |
| samtools/htsjdk |
271 |
|
170 |
87 |
over 2 years ago |
78 |
October 13, 2023 |
303 |
|
Java |
| A Java API for high-throughput sequencing data (HTS) formats. |
| igordot/genomics |
154 |
|
0 |
0 |
over 3 years ago |
0 |
|
2 |
|
R |
| A collection of scripts and notes related to genomics and bioinformatics |
| chrovis/cljam |
87 |
|
0 |
0 |
about 2 years ago |
37 |
May 10, 2019 |
6 |
apache-2.0 |
Clojure |
| A DNA Sequence Alignment/Map (SAM) library for Clojure |
| apriha/snps |
82 |
|
1 |
2 |
about 2 years ago |
42 |
June 06, 2022 |
23 |
bsd-3-clause |
Python |
| tools for reading, writing, merging, and remapping SNPs |
| hdeweyh/strangerVisions |
35 |
|
0 |
0 |
over 9 years ago |
0 |
|
2 |
gpl-3.0 |
Python |
| biosinodx/SCcaller |
28 |
|
0 |
0 |
over 3 years ago |
0 |
|
3 |
agpl-3.0 |
Python |
| Single Cell Caller (SCcaller) - Identify single nucleotide variations (SNVs) from single cell sequencing data |
| biowdl/germline-DNA |
23 |
|
0 |
0 |
almost 3 years ago |
0 |
|
2 |
mit |
wdl |
| A BioWDL variantcalling pipeline for germline DNA data. Starting with FASTQ files to produce VCF files. Category:Multi-Sample |
| qtao/Genomic-Data-Science |
17 |
|
0 |
0 |
over 10 years ago |
0 |
|
0 |
|
HTML |
| Genomic data science specialization |
