Visual for Bioinformatics
Quickly identify disease-causing variants
When analyzing data from DNAseq studies, CLC Genomics Workbench and Ingenuity Variant Analysis provide the fastest time to accurate insights. Only the combination of CLC Genomics Workbench and Ingenuity Variant Analysis enables you to proceed with confidence knowing your processed data is accurate, allowing you to make impactful discoveries using the largest repository of curated biological findings.
For analyzing, comparing, and visualizing next-generation sequencing data
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A high-performance computing solution for mapping reads to a reference and de novo assembly of next-generation sequencing data.
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For flexible next-generation sequencing data analysis
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For advanced DNA, RNA, and protein analyses
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For enhancing functionalities of CLC Genomics Workbench, Biomedical Genomics Workbench, and CLC Server solutions
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For identifying disease-causing variants from human whole genome, exome and gene panel next-generation sequencing studies
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