VarSeq Software

VarSeq® software streamlines the process of annotating and filtering variants obtained from next generation sequencing pipelines, allowing both research scientists and clinicians to find variants of interest in a very efficient and straightforward manner. VarSeq simplifies the user interface and provides a scalable architecture featuring repeatable workflows, note taking and reporting, and filter parameter prototyping.

Download VarSeq

Resources


Getting Started:
Install and Login Guide

Everything you need to know about how to install VarSeq, create a login and register the product.


Getting Started:
Creating a New Project

Walks you through creating a new project, annotating and filtering variants and exporting filtered and annotated data.


Getting Started:
Work with an Existing Project

Quickly learn how to manipulate the visible data and samples, adjust the layout of the views in the project and take notes that are saved as part of the project.

Getting Started:
GenomeBrowse

Get up and running with the embedded genome browser, adding plots, navigating to features and changing how data is displayed.


VarSeq Manual

Read the full VarSeq manual to learn all about the product and its features!

Tutorial: Introduction to Varseq

This tutorial covers a basic de Novo Trio workflow with an emphasis on understanding and exploring filter chains and variant tables

Tutorial: Cancer Gene Panel

This tutorial covers a basic gene panel workflow with an emphasis on adding, modifying and manipulating filter chains.



VarSeq ® Software is intended for Investigational Use Only. The performance characteristics of this product have not been established.