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NGS variant analysis software

Collection: Bioinformatics

NGS bioinformatics in Israel: variant analysis and interpretation software (VarSome, SOPHiA DDM) and sequencing kits that come with their analysis and reporting (Illumina TruSight Oncology 500 with Connected Insights or a Velsera report).

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93 products

VarSome Clinical NGS Variant Analysis and Interpretation Platform (VARSOME-CLINICAL)

VarSome Editions

VarSome Clinical NGS Variant Analysis and Interpretation Platform

Regular price 0.00 NIS
Sale price Regular price
SOPHiA DDM Platform - secure login and FASTQ data upload screen - SOPHiA GENETICS

Software Platform

SOPHiA DDM™ Platform

Regular price 0.00 NIS
Sale price Regular price
VarSome Premium Variant Search and Annotation Subscription (VARSOME-PREMIUM)

VarSome Editions

VarSome Premium Variant Search and Annotation Subscription

Regular price 0.00 NIS
Sale price Regular price
TruSight Oncology 500 High-Throughput DNA for Automation (144 Samples) 20049285 - Illumina

Clinical research products

TSO500 DNA/RNA HT Auto (72 spls) + Velsera

Regular price 61,227.00 NIS
Sale price Regular price
TruSight Oncology 500 High-Throughput DNA for Automation (144 Samples) 20049285 - Illumina

Clinical research products

TruSight Oncology 500 DNA High-Throughput Kit (144 Samples), plus Velsera

Regular price 71,585.00 NIS
Sale price Regular price

Buying Guide

Start from where your analysis happens. To call and interpret variants from your own FASTQ or VCF files, use VarSome Clinical (CE-IVDR) or the SOPHiA DDM Platform; for looking up single variants, a VarSome Premium seat is enough. If you also need the wet-lab kit, SOPHiA DDM solutions bundle the capture panel with its analysis, and Illumina TruSight Oncology 500 kits come with Illumina Connected Insights software or a Velsera interpretation report.