The @AllofUsResearch Program has gathered diverse genomic data on a large scale, identifying over 275 million new genetic variants to enhance precision medicine. Nanopore sequencing technology offers comprehensive analysis of various genetic elements, including SNVs, SVs, CNVs, STRs, and more. Xingli @firXLLi showcased Nanopore sequencing using SigmaFacto's P2 machine for genome analysis. Nanopore sequencing is being utilized for genome assembly, genetic diversity insights, DNA methylation, and other genetic studies. Rapid genome sequencing and targeted analysis are being employed for quick genetic risk assessment in medicine.
3-hour genome sequencing and targeted analysis to rapidly assess genetic risk. #RapidGenomeSequencing @nanopore #TargetedGeneticAnalysis #GeneticsinMedicineOpen https://t.co/rkRKm9CJLN
Have you used #nanopore sequencing for genome assembly, insights into genetic diversity, DNA #methylation, phasing, #transcriptomics, #epitranscriptomics, or metagenomics? Don't miss you chance to feature in a special Issue in Biology and Medicine. ⬇️https://t.co/hOXLr55UyB
Xingli @firXLLi demonstrated Nanopore sequencing using our P2 machine. https://t.co/qW1RUtvfQ6
Unlock the full potential of multiomics without the complexity. Nanopore sequencing offers a comprehensive analysis. Dive into the details of SNVs, SVs, CNVs, STRs, haplotyping, & methylation alongside RNA isoforms, in one platform. Learn more: https://t.co/oas0KbISAk #WYMM https://t.co/uxZ0uxx5GY
An @AllofUsResearch Program resource describes diverse #genomic data collected at unprecedented scale—identifying more than 275 million new genetic variants. This data aims to improve implementation of precision medicine for everyone. @AlexBickMDPhD @NIH https://t.co/cQNCRJdJZZ https://t.co/Z8YvDUnaGQ