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.
The ClearSeq Cancer research panels are the industry-leading cancer profiling solution for pathologists seeking to use NGS to understand solid and hematological tumors.
SureDesign is intuitive design software which enables users to create custom target enrichment libraries and microarrays that focus specifically on their gene targets.
SureCall software allows clinical researchers to transform raw NGS data into insights without bioinformatics training or advanced infrastructure.
Amplify multiple genomic targets in a single PCR experiment
Here are educational resources to aid in the accurate and comprehensive identification of somatic variants in solid tumors and hematological cancers.
The NGS Bravo offers the advantages of increasing throughput without affecting data quality and freeing up researchers from performing time consuming, repetitive tasks.
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