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463
other
9
Efficient pythonic random access to fasta subsequences
Created 2013-09-12
879 commits to master branch, last one 2 months ago
82
414
other
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The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
Created 2016-04-04
6,845 commits to main branch, last one a day ago
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227
mit
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WebAssembly modules for genomics
Created 2019-09-07
1,193 commits to main branch, last one 17 days ago
Work with bioinformatic files using Arrow, Polars, and/or DuckDB
Created 2023-04-22
299 commits to main branch, last one 6 days ago
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A modern compressor for genomic files (FASTQ, SAM/BAM/CRAM, VCF, FASTA, GFF/GTF/GVF, 23andMe...), up to 5x better than gzip and faster too
Created 2019-12-15
3,265 commits to master branch, last one 15 days ago
NGLess: NGS with less work
Created 2013-01-08
2,453 commits to main branch, last one 4 months ago
Learning the Sequence Alignment/Map format
Created 2016-04-15
94 commits to main branch, last one 9 months ago
Multi-sample somatic variant caller
Created 2015-06-16
981 commits to master branch, last one 5 years ago
Here we are going to discuss variant calling on human datasets using GATK Best practices pipeline
Created 2023-12-22
69 commits to main branch, last one 11 months ago