Detection of Structural Variants in Targeted Sequencing
Abstract
Structural Variants (SVs) have long been implicated in many human diseases such as cancer, making their detection important in clinical genomics. Strand NGS 2.5 includes a new workflow step for detecting these variants based on split reads that span the breakpoints corresponding to the variants. Detection of SVs using split reads provides breakpoints with a higher precision compared to the methods based on paired-end reads. In this webinar, we will describe this method and demonstrate its application to detection of somatic gene fusions in targeted sequencing data. We will also show how the detected SVs can be visually validated in the elastic genome browser of Strand NGS.
Webinar Details
| Sessions | San Francisco Time (PDT) |
Tokyo Time (GMT+09:00) |
Berlin Time (GMT+01:00) |
Mumbai Time (GMT+05:30) |
| Session 1 | 30 Sep 01:30 AM |
30 Sep 05:30 PM |
30 Sep 10:30 AM |
30 Sep 02:00 PM |
| Session 2 | 30 Sep 09:00 AM |
01 Oct 01:00 AM |
30 Sep 06:00 PM |
30 Sep 09:30 PM |
