bedtools - the swiss army knife for genome arithmetic
Foundation Models for Genomics & Transcriptomics
The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
Burrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.
The second version of the Kraken taxonomic sequence classification system
Official git repository for Biopython (originally converted from CVS)
Oxford Nanopore's Basecaller
Tools (written in C using htslib) for manipulating next-generation sequencing data
Single-cell analysis in Python. Scales to >100M cells.
Official code repository for GATK versions 4 and up
C library for high-throughput sequencing data formats
A comprehensive library for computational molecular biology
The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants
IQ-TREE software version 2: phylogenetics by maximum likelihood
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
📖🔬☕ BioJava is an open-source project dedicated to providing a Java library for processing biological data.
A versatile pairwise aligner for genomic and spliced nucleotide sequences
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