The preprint is out! A highly accurate framework to simultaneous assess all genome #variants (SNV, indels, STR, SV & CNV) at scale: #DRAGEN @illumina Evaluated, Benchmarked and explained by the Sairam Behera and Fritz Sedlazeck's collaborating with the #DRAGEN team. https://lnkd.in/gsyA_YiW #sequencing #bioinformatics
Awesome work! Is the local reassembly of active regions taking place on FPGA?
Great to see how far we've come with secondary analysis, especially for difficult regions/variants. Congrats to the Dragen team!
This is amazing! Awesome work demonstrating, explaining and comparing DRAGEN's capabilities by all the authors
Congrats Rami, Sairam, Fritz and the DRAGEN team. Truly impressive and innovative methods for comprehensive germline variant calling using multi-genome graphs. The hardware/software speed and scale optimization is equally impressive. Well done!
Congratulations to the team Rami Mehio !
Congrats Rami and team!
Fabulous work! We’re all grateful for your hard work and expertise. 😀
CEO & Founder @ Geneial | Genomics | Data | Precision Medicine | Entrepreneur
8moExciting! Any plans or recommendations for star allele variant calling in the works as well?