Illumina reanalyzed the 1000 Genomes Project using DRAGEN v4.4 on AWS EC2 to establish an updated analytical baseline for human genetic variation, now publicly available with pangenome-based variant calling and natural language query capabilities.

Direct enzymatic fragmentation of genomic DNA with NEBNext UltraShear for use with Illumina 5-Base DNA Library Prep without post-shearing cleanup. . Read ful...

Deliver unbiased whole‑transcriptome sequencing with true cellular‑level spatial resolution in intact tissue sections for any eukaryotic species.

Gain a deeper understanding of the genome and epigenome with the Illumina 5‑Base Solution for Cancer Research Grant Contest

A head-to-head comparison evaluated WGS using the MGI DNBSEQ-T7 sequencing platform with MegaBOLT v2.4.0 software against the NovaSeq X Series with DRAGEN v4.4 software.

YouTube video by Illumina

DRAGEN rapidly identifies diverse types of genetic variants.

Discover how the Illumina 5-base solution and DRAGEN pipeline streamline genetic and epigenetic analysis with accurate methylation and variant insights.

⚡♠️ Assemble bacterial isolate genomes from Illumina paired-end reads - tseemann/shovill

The South African Medical Research Council (SAMRC) and the Department of Science, Technology and Innovation (DSTI) have taken another major step toward advancing genomic and precision medicine researc...

Despite significant advances in genomic sequencing, the resolution of many rare disease cases is still hindered by variant detection limitations. Short reads struggle in homologous regions, and long r...