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Bayesian haplotype-based genetic polymorphism discovery and genotyping.
fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
ChIP-seq analysis notes from Ming Tang
Hifiasm: a haplotype-resolved assembler for accurate Hifi reads
A fast and sensitive gapped read aligner
Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
A Go package for engineering organisms.
A single molecule sequence assembler for genomes large and small.
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings
Rapid & standardized annotation of bacterial genomes, MAGs & plasmids
Create an index on a compressed text file
:book::microscope::coffee: BioJava is an open-source project dedicated to providing a Java library for processing biological data.
A quality control analysis tool for high throughput sequencing data
Yet another redundant workflow engine
Another Gtf/Gff Analysis Toolkit https://nbisweden.github.io/AGAT/
Mummer alignment tool
A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.
SIFT
DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
Redbean: A fuzzy Bruijn graph approach to long noisy reads assembly
A flexible pipeline for complete analysis of bacterial genomes
The Leek group guide to genomics papers
🔬A library of JavaScript components to represent biological data
Efficient pythonic random access to fasta subsequences
RSEM: accurate quantification of gene and isoform expression from RNA-Seq data
JBrowse 1, a full-featured genome browser built with JavaScript and HTML5. For JBrowse 2, see https://github.com/GMOD/jbrowse-components.
Structural variant and indel caller for mapped sequencing data
The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
cython + htslib == fast VCF and BCF processing
C++ API & command-line toolkit for working with BAM data