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NGS Solutions for Pathology

With increasing understanding about the genetic changes that occur in cancer, now you can interrogate driver mutations in parallel, saving critical time to answers. Our portfolio includes catalog and custom NGS gene panels, analysis software, and automation systems which facilitate parallel analysis, substantially reducing the time to answer.

ClearSeq Cancer Research Panels

The ClearSeq Cancer research panels are the industry-leading cancer profiling solution for pathologists seeking to use NGS to understand solid and hematological tumors.

ClearSeq Cancer Research Panels

SureDesign Custom Design Software

SureDesign is intuitive design software which enables users to create custom target enrichment libraries and microarrays that focus specifically on their gene targets.

SureDesign Custom Design Software

SureCall Software

SureCall software allows clinical researchers to transform raw NGS data into insights without bioinformatics training or advanced infrastructure.

SureCall Software

Amplicon Target Amplification (Multiplicom)

Amplify multiple genomic targets in a single PCR experiment

Learn more about Amplicon Target Amplification (Multiplicom)

NGS Cancer Research Resources Center

Here are educational resources to aid in the accurate and comprehensive identification of somatic variants in solid tumors and hematological cancers.

NGS Cancer Research Resources Center

NGS Sample Preparation Automation

The NGS Bravo offers the advantages of increasing throughput without affecting data quality and freeing up researchers from performing time consuming, repetitive tasks.

NGS Sample Preparation Automation

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Solutions for Pathology