Modern and easy to use SQL client for MySQL, Postgres, SQLite, SQL Server, and more. Linux, MacOS, and Windows.

ExomeDepth R package for the detection of copy number variants in exomes and gene panels using high throughput DNA sequencing data.

Regulatory Tables for Clinical Research

Collection of bioinformatics training materials

Copy Number Variation Detection In Next-generation sequencing Gene panels was designed for small (single-exon) copy number variation (CNV) detection in high coverage next-generation sequencing (NGS…

Copy number calling and variant classification using targeted short read sequencing

CNV detection tool for targeted NGS panel data

Copy number variant detection from targeted DNA sequencing

Clone of the Bioconductor repository for the scRNAseq package.

Various algorithms for analysing genomics data

IMGT segment library converted to RepSeq.IO JSON format

MiXCR is an ultimate software platform for analysis of Next-Generation Sequencing (NGS) data for immune profiling.

GRIDSS: the Genomic Rearrangement IDentification Software Suite

A repo with random short code snippets

Explore design matrices interactively with R/Shiny

checkcites is a Lua script written for the sole purpose of detecting undefined/unused references from LaTeX auxiliary or bibliography files.

Toolkit for processing sequences in FASTA/Q formats