Emedgene software

18 Mar 2026

In this data sheet, Illumina highlights Emedgene™, a research software designed to streamline variant interpretation workflows for next-generation sequencing applications. Emedgene integrates with Illumina secondary analysis and data platforms, including DRAGEN™ Secondary Analysis, and accepts input from WGS, WES, targeted panels, and microarrays, covering comprehensive variant types for streamlined research report generation.

DRAGEN™

Illumina

A suite of bioinformatics pipelines to process NGS data and maximise genomic discovery.

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Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.
Emedgene software