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The CytoSure® Constitutional NGS solution delivers robust CNV analysis down to single-exon level and loss of heterozygosity (LOH) as well as SNV and indel detection, all in a single assay.
In addition to SNVs and indels, the SureSeq™ CLL + CNV Panel also accurately detects small and large CNVs, trisomy 12 and LOH, to obtain a more complete understanding of the genetic makeup of your CLL research samples in a single NGS assay.
This poster provides a quick guide to abnormal results expected from our line of FDA-cleared FISH probes for AML and MDS.
We understand that making the change from aCGH to NGS is a daunting prospect, particularly when it comes to data analysis.
That’s why we’ve developed Interpret NGS analysis software for use in conjunction with the CytoSure Constitutional NGS panel for constitutional cytogenetics research.
Presented at AMP 2019, this poster demonstrates the capability of the SureSeq CLL + CNV panel to overcome the challenges of detecting CNVs in CLL samples.
Learn how to track the progress of a case in the Case Status field. The video details the various stages, transitioning between them and how the function can be used to search for samples in database management.
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