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Awesome List
A curated list of awesome Bioinformatics libraries and software.
GitHub stars and default-branch commits for danielecook/Awesome-Bioinformatics.
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Official git repository for Biopython (originally converted from CVS)
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
A versatile pairwise aligner for genomic and spliced nucleotide sequences
Burrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Cloud-native genomic dataframes and batch computing
Hifiasm: a haplotype-resolved assembler for accurate Hifi reads
A fast and sensitive gapped read aligner
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings
:book::microscope::coffee: BioJava is an open-source project dedicated to providing a Java library for processing biological data.
Efficient pythonic random access to fasta subsequences
JBrowse 1, a full-featured genome browser built with JavaScript and HTML5. For JBrowse 2, see https://github.com/GMOD/jbrowse-components.
cython + htslib == fast VCF and BCF processing
annotate a VCF with other VCFs/BEDs/tabixed files
fast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
Bayesian haplotype-based mutation calling
Reads simulator
structural variant calling and genotyping with existing tools, but, smoothly.
Blazing-Fast Bioinformatic Operations on Python DataFrames
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
:rocket: seqfu - Sequece Fastx Utilities
Explore and analyze biological sequence data