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A translator from Intel SSE intrinsics to Arm/Aarch64 NEON implementation

A simple and efficient tool to parallelize Pandas operations on all available CPUs

A DSL for data-driven computational pipelines

ProSolo, variant calling from single cell DNA-seq data, or: bulk backing vocals for single cell solos.

code and manuscript of "ProSolo: Accurate Variant Calling from Single Cell DNA Sequencing Data"

Official repository for Citation Style Language (CSL) citation styles.

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

A pure-python implementation of the UpSet suite of visualisation methods by Lex, Gehlenborg et al.

Vector class library, latest version

Human Pangenome Reference Consortium - HG002 Data Freeze (v1.0)

Community-curated list of software packages and data resources for single-cell, including RNA-seq, ATAC-seq, etc.

Data and information about the Polaris study

Demographic inference from whole genomes

The next version of bwa-mem

fast log and exp functions for AVX2/AVX-512

2 ~ 6 sets venn diagram for python

Validation runs using bcbio: germline, somatic, structural variant calling and RNA-seq analyses

Statistical data visualization in Python

software tools for haplotype assembly from sequence data

LaTeX template for an Oxford University thesis

Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations

A flexible variational inference LDA library.

A Fast Implementation of Random Forests

Specifications of SAM/BAM and related high-throughput sequencing file formats

scikit-learn: machine learning in Python

mlpack: a fast, header-only C++ machine learning library

Deep Learning for humans