Exome sequencing is a capture-based method that targets and sequences coding regions of the genome, referred to as ‘the exome’. In contrast, genome sequencing doesn’t require a capture step and offers coverage across the entire genome. While most of the interpretable genome falls within the exome, genome sequencing is capable of detecting additional clinically relevant variation.

Whole Exome Sequencing | Patient Guide

There are many different legislative statutes that govern service delivery and may be difficult to navigate for individuals and families who are new to California or to the regional center system.

Targeted sequencing to detect exonic variants

Analyze the protein-coding regions of the genome to uncover genetic influences on disease and population health.

What are whole exome sequencing and whole genome sequencing?

. . .DNA sequencing, has advanced the study of genetics and is one technique used to test for genetic disorders.

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants