SBGrid Consortium homepage

UGENE is a free open-source bioinformatics software for macOS, and Linux.

SAIGE is an R package developed with Rcpp for genome-wide association tests in large-scale data sets and biobanks.

a flexible dynamic language appropriate for scientific and numerical computing with performance comparable to traditional statically-typed languages.

a C++ program for whole genome regression modelling of large genome-wide association studies.

a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed.

(Sequence Alignment/Map) a generic format for storing large nucleotide sequence alignments that provides various utilities for manipulating alignments, including sorting, merging, indexing and generating alignments in a per-position format.

a reference-free whole-genome multiple alignment program based upon notion of Cactus graphs.

(Genome Analysis Toolkit) a software package developed to analyze high-throughput sequencing data capable of taking on projects of any size with a primary focus on variant discovery, genotyping, and data quality assurance.

an ultra fast and sensitive sequence search and clustering suite

Cellpose-SAM: cell and nucleus segmentation with superhuman generalization. It can be optimized for your own data, applied in 3D, works on images with shot noise, (an)isotropic blur, undersampling, contrast inversions, regardless of channel order and object sizes.