Welcome to Answer’s documentation!

ANSWER can be used by clinical geneticists or pathologists to identify clinically actionable variants from next-generation sequencing data for the purposes of recommending personalized treatment options.

Functions

The platform allows users to * examine variant quality using the integrated genome viewer (IGV) * add their own annotations that can be used in future cases * filter variants based on their gene location, chromosomal feature or quality metrics * generate a clinical report in PDF format or HL7 format that can be loaded into the providers electronic health record (EHR)