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I improve human lives
by creating software
for biologists and clinicians
to accelerate breakthroughs in genomics science

Nils Homer's Projects

pyd4 icon pyd4

The python binding for D4 format

pysam icon pysam

Pysam is a Python module for reading and manipulating SAM/BAM/VCF/BCF files. It's a lightweight wrapper of the htslib C-API, the same one that powers samtools, bcftools, and tabix.

pyvcf icon pyvcf

A Variant Call Format reader for Python.

riboseqc icon riboseqc

Pipeline for Quality Control of Ribo-Seq data, selection of P-site offsets, and codon usage statistics.

rsem icon rsem

RSEM: accurate quantification of gene and isoform expression from RNA-Seq data

rust-bio icon rust-bio

This library provides implementations of many algorithms and data structures that are useful for bioinformatics. All provided implementations are rigorously tested via continuous integration.

rust-htslib icon rust-htslib

This library provides HTSlib bindings and a high level Rust API for reading and writing BAM files.

samblaster icon samblaster

samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.

samwell icon samwell

Samwell: a python package for using genomic files... well

sga icon sga

experimental de novo sequence assembler using string graphs

snakemake icon snakemake

This is the development home of the workflow management system Snakemake. For general information, see

snakeparse icon snakeparse

Making Snakemake workflows into full-fledged command line tools since 1999.

somalier icon somalier

fast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"

spoa icon spoa

SIMD partial order alignment tool/library

squid icon squid

SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data

srma icon srma

Short-read Micro-Aligner

staged-recipes icon staged-recipes

A place to submit conda recipes before they become fully fledged conda-forge feedstocks

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