A streamlined, automated process helps scientists coordinate site-ready production-level whole genome sequencing results.

Structural variations (SVs)—large-scale changes in DNA sequence—play a crucial role in shaping traits such as yield, quality, and environmental adaptation in crops.

A new CRISPR approach can control genes without cutting DNA, opening a safer path for treating genetic diseases. A newly ...

Researchers have uncovered nearly 150 hidden DNA “switches” inside brain support cells that control the activity of genes ...

Artificial intelligence has just redrawn the map of our genome’s control room, revealing hundreds of thousands of tiny DNA ...

AI maps fleeting DNA quadruplexes, revealing paired structures that control genes in healthy cells and cancer.

Our DNA to Amino Acid Converter helps you translate genetic sequences into protein structures quickly and easily. You can use it with standard or specialised genetic codes, and it accepts DNA or RNA ...

Pull requests help you collaborate on code with other people. As pull requests are created, they’ll appear here in a searchable and filterable list. To get started, you should create a pull request.

This repository provides simple bioinformatics tools for reading FASTQ and FASTA files, building k-mer overlap graphs for genome assembly, and performing pattern matching using edit distance for ...

Researchers at EMBL’s European Bioinformatics Institute (EMBL-EBI) have developed a new machine learning method called SAVANA that significantly reduces sequencing errors for cancer genomes. Long-read ...