Editorial: Next generation sequencing (NGS) for rare diseases diagnosis - Volume II

Xiu-An Yang; Hu Hao; Can Liao

doi:10.3389/fgene.2023.1249585

Editorial: Next generation sequencing (NGS) for rare diseases diagnosis - Volume II

Front Genet. 2023 Jul 10:14:1249585. doi: 10.3389/fgene.2023.1249585. eCollection 2023.

Authors

Xiu-An Yang^{1

2}, Hu Hao^{3

4}, Can Liao⁵

Affiliations

¹ Laboratory of Genetic Engineering and Genomics, School of Basic Medical Sciences, Chengde Medical University, Chengde, China.
² Hebei Key Laboratory of Nerve Injury and Repair, Chengde Medical University, Chengde, China.
³ Department of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
⁴ Inborn Errors of Metabolism Laboratory, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
⁵ Guangzhou Women and Children's Medical Center, Guangzhou, China.

No abstract available

Keywords: copy number variants (CNV) sequencing; next generation sequencing; rare diseases diagnosis; whole-exome sequencing; whole-genome sequencing.

Publication types

Editorial

Grants and funding

This study was supported by Natural Science Foundation of Hebei Province (No. H2020406049), Scientific and Technological Research Projects of Hebei Higher Education (No. ZD2019084), and Initial Scientific Research Fund for High-Level Talents of Chengde Medical University (No. 201901).