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