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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

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Hereditary Cancers

SOPHiA DDM™ Dx Hereditary Cancer Solution (CE-IVD)

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Solid Tumors

SOPHiA DDM™ Solid Tumor Plus Solution (STS+)

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Blood Cancers

SOPHiA DDM™ Myeloid Solution (MYS)

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Solid Tumors

SOPHiA DDM™ Dx Homologous Recombination Deficiency Solution (CE-IVD)

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Blood Cancers

SOPHiA DDM™ Myeloid Plus Solution (MYS+)

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Blood Cancers

SOPHiA DDM™ Dx Myeloid Solution (CE-IVD)

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Liquid Biopsy

MSK-ACCESS® powered with SOPHiA DDM™

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Inherited Disorders

SOPHiA DDM™ Nephropathies Solution

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Rare Disorders

SOPHiA DDM™ Clinical Exome Solution v3 (CES v3)

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Blood Cancers

SOPHiA DDM™ Extended Myeloid Plus Solution (ExtMYS+)

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Rare Disorders

SOPHiA DDM™ Enhanced Clinical Exome Solution

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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.