Posted On: Feb 5, 2024
Today, AWS HealthOmics expands its Ready2Run workflows with Ultima Genomics DeepVariant Ready2Run workflow, which is designed to perform variant calling from whole genome sequencing data generated on Ultima Genomics UG100 sequencing instrument. With this release, customers can now bring their own CRAM files and use Ultima Genomics DeepVariant Ready2Run workflow to generate a single-sample whole genome gVCF or VCF of the variants.
AWS HealthOmics is a fully managed service that helps healthcare and life science organizations and their software partners store, query, and analyze genomic, transcriptomic, and other omics data and then generate insights from that data to improve health and advance scientific discoveries. The new Ultima Genomics DeepVariant Ready2Run workflow enables customers to easily run variant calling on their whole genome sequencing data without the burden of building and maintaining the infrastructure needed to run these complex analysis pipelines. This saves significant time and effort while producing high-quality results.
Ultima Genomics DeepVariant Ready2Run workflow is supported in the following AWS HealthOmics regions: US East (N. Virginia), US West (Oregon), Europe (Frankfurt, Ireland, London), and Israel (Tel Aviv). Visit the AWS HealthOmics console to learn more and get started with Ultima Genomics DeepVariant Ready2Run workflow on AWS HealthOmics.