Academic Paper - CompStor Novos®: low cost yet fast assembly-based variant calling for personal genomes
OmniTier's in-press paper on CompStor Novos with Mayo Clinic collaborators.
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Application Note # 1 - High Accuracy Variant Calling
CompStor Novos® variant calling well exceeds standard open source solutions
Application Note # 2 - precisionFDA Winning Accuracy Results
CompStor Novos® surpasses commercial solutions in the precisionFDA Truth Challenge
Product Brief - Insight Hereditary
Insight Hereditary is germline, hereditary and rare disease tertiary analysis software that runs on OmniTier’s CompStor Server platform, either on-premise, in an HPC or in a private cloud. Insight Hereditary can analyze single, duo, trio or larger family collections of gene panels, WES or WGS .vcfs. Outputs can either be draft or final causal reports of prioritized, classified, pathogenic and likely pathogenic variants, or cohorts of samples can be analyzed using GWAS.
Benchmarking End-to-End, On-Premise, WGS Analysis, using Sentieon DNAscope Secondary Analysis with OmniTier Insight Tertiary Analysis
Integration of the Sentieon DNAscope secondary analysis software into OmniTier’s CompStor Workgroup server enabled end-to-end analysis of Illumina, PacBio and Oxford Nanopore WGS data, on a single mid-range CPU based rack server. The speed optimization during the development of both DNAscope and Insight results in short end-to-end runtimes, whilst keeping accuracy high.These good test results demonstrate that this is a good solution for those customers seeking an on-premise, end-to-end analysis solution.
Product brief - CompStor Novos
CompStor Novos® Pro is an accelerated, human genome secondary analysis, on-premise appliance for WGS, WES and targeted gene panels. Supporting short and long read sequencers. Fast analysis times using proprietary technology provides low cost per genome. Proprietary, highly accurate variant calling is driven by a domain specific, deep learning algorithm, in addition to standard GATK.