Streamlined NGS Analysis for CNV Identification
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Targeted next-generation sequencing (NGS) is increasingly being adopted into laboratories for genomic testing. These tests are particularly important for researching somatic and germline variants like those linked to cancer.
However, while the detection of single nucleotide variations (SNVs) and insertions and deletions (indels) is well established, it is still challenging to accurately identify exon-level copy number variations (CNVs).
This application note explores the use of an intuitive and streamlined solution for NGS analysis of a broad range of CNVs.
Download this application note to discover:
- A quick and easy NGS analysis platform
- A streamlined workflow for efficient variant calling
- Enhanced CNV detection accuracy
Research Use Only. Not for use in diagnostic procedures.
Agilent
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