We are shortly approaching the public launch (November 5th!) of our first clinical product, VarSeq. We could not have predicted how well the market would accept VarSeq – but we couldn’t be happier! For those of you who have not yet seen our newest product in action, I invite you to register for tomorrow’s webcast: The Golden Helix VarSeq User Experience.
On Wednesday November 5th, Dr. Bryce Christensen, Statistical Geneticist from Golden Helix will host a webcast presenting VarSeq from the analyst’s perspective. Topics will include data import, annotation and filtering, creation and application of custom workflows, interactive data exploration, and customization of the VarSeq user interface. Interactive examples will be shown based on gene panels and exome sequencing.
VarSeq software streamlines the annotation and variant filtering process obtained from next generation sequencing pipelines, allowing both research scientists and clinicians to find variants of interest in a very efficient and straightforward manner. The software also simplifies the user interface and provides a scalable architecture featuring repeatable workflows, note taking and reporting, and filter parameter prototyping.
You can register for the webcast at: https://www2.gotomeeting.com/register/762642714.
We hope to “see” you there!