copy number variants

3 min read 2021-04-09 03:35:00

Webcast Recap: Exome Analysis with VS-CNV and VSClinical: Updated Strategies and Expanded Capabilities

Thank you to those who attended the recent webcast, “Exome Analysis with VS-CNV & VSClinical: Updated Strategies & Expanded

4 min read 2020-10-23 03:24:00

Golden Helix is excited to release an upcoming VSClinical feature that allows users to analyze next-generation sequencing (NGS) CNV event reporting

4 min read 2020-08-20 16:00:00

Our software solutions and partners have brought dramatic improvements to the secondary and tertiary analysis stages of variant evaluation. Regarding

4 min read 2020-08-15 00:32:27

It doesn’t take much effort to find articles discussing the value of Next-Generation Sequencing (NGS). There is a consistent tone amongst authors

4 min read 2019-10-18 20:01:43

Comparison of early Homo sapiens with Homoneanderthalensis. Credit: Wikipedia. One of the most interesting questions of hominin evolution is

4 min read 2019-10-11 05:18:07

The common approaches to detecting copy number variants (CNVs) are chromosomal microarray and MLPA. However, both options increase analysis time, per

1 min read 2016-05-05 02:58:00

This blog was inspired by discussions I have been having with Allen Frances and also partly in response to some blogs he was written about the role