Nils Homer's Projects
A conda-smithy repository for prometheus.
The python binding for D4 format
A conda-smithy repository for pyhocon.
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.
A Variant Call Format reader for Python.
AWS Quick Start Team
AWS Quick Start Team
Example Read Structures for BAM <-> FASTQ
Pipeline for Quality Control of Ribo-Seq data, selection of P-site offsets, and codon usage statistics.
RSEM: accurate quantification of gene and isoform expression from RNA-Seq data
This library provides implementations of many algorithms and data structures that are useful for bioinformatics. All provided implementations are rigorously tested via continuous integration.
A library of common biomedical types.
This library provides HTSlib bindings and a high level Rust API for reading and writing BAM files.
Single-Cell RNA-seq pseudo-aligner
samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.
Samwell: a python package for using genomic files... well
Sbt plugin for uploading Scala code coverage to coveralls
experimental de novo sequence assembler using string graphs
This is the development home of the workflow management system Snakemake. For general information, see
Snakemake with pytest example
Making Snakemake workflows into full-fledged command line tools since 1999.
Making snakemake wrappers cool again
fast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
SIMD partial order alignment tool/library
SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data
Short-read Micro-Aligner
A place to submit conda recipes before they become fully fledged conda-forge feedstocks