Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar

Next generation sequencing (NGS) technologies such as whole genome and whole exome sequencing has enabled accurate diagnosis of genetic diseases through identification of variations at the genome wide level. While many large populations have been adequately covered in global sequencing efforts littl...

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Bibliographic Details
Main Authors: Abhinav Jain, Shrey Gandhi, Remya Koshy, Vinod Scaria
Format: Article
Language:English
Published: Science Planet Inc. 2017-10-01
Series:Canadian Journal of Biotechnology
Online Access:https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue/cjb.2017-a67.pdf