Making NGS Data Analysis Clinically Practical: Repeatable and Time-Effective Workflows





The interactive transcript could not be loaded.


Rating is available when the video has been rented.
This feature is not available right now. Please try again later.
Published on Sep 11, 2013

Exploring next-generation sequence data requires an iterative process whereby a researcher can find a "needle in the haystack" that contributes to a particular disease or other phenotype. Once that needle has been found, a workflow can be established for analyzing other samples or to create a repeatable, time-effective process for clinical usage.

Yet, repeating a workflow that involves several different quality control, filtering, and analysis steps is burdensome and error-prone.

To solve this problem, we introduce custom workflow automation in SVS, which allows you to collapse dozens of steps into a few run-specific options. This click-and-go process saves an exponential amount of time while eliminating the inevitable user error that happens with tedious repetition and ensures that the exact same protocol is followed with each run, a critical requirement for use in the clinic.



When autoplay is enabled, a suggested video will automatically play next.

Up next

to add this to Watch Later

Add to

Loading playlists...