Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2023-07-01
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| Series: | Frontiers in Genetics |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2023.1249585/full |
| _version_ | 1797783816710914048 |
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| author | Xiu-An Yang Xiu-An Yang Hu Hao Hu Hao Can Liao |
| author_facet | Xiu-An Yang Xiu-An Yang Hu Hao Hu Hao Can Liao |
| author_sort | Xiu-An Yang |
| collection | DOAJ |
| first_indexed | 2024-03-13T00:31:14Z |
| format | Article |
| id | doaj.art-a92de7dcdc6b43ed9097cebfcd68abae |
| institution | Directory Open Access Journal |
| issn | 1664-8021 |
| language | English |
| last_indexed | 2024-03-13T00:31:14Z |
| publishDate | 2023-07-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Genetics |
| spelling | doaj.art-a92de7dcdc6b43ed9097cebfcd68abae2023-07-10T13:29:00ZengFrontiers Media S.A.Frontiers in Genetics1664-80212023-07-011410.3389/fgene.2023.12495851249585Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume IIXiu-An Yang0Xiu-An Yang1Hu Hao2Hu Hao3Can Liao4Laboratory of Genetic Engineering and Genomics, School of Basic Medical Sciences, Chengde Medical University, Chengde, ChinaHebei Key Laboratory of Nerve Injury and Repair, Chengde Medical University, Chengde, ChinaDepartment of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, ChinaInborn Errors of Metabolism Laboratory, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, ChinaGuangzhou Women and Children’s Medical Center, Guangzhou, Chinahttps://www.frontiersin.org/articles/10.3389/fgene.2023.1249585/fullnext generation sequencingrare diseases diagnosiswhole-exome sequencingwhole-genome sequencingcopy number variants (CNV) sequencing |
| spellingShingle | Xiu-An Yang Xiu-An Yang Hu Hao Hu Hao Can Liao Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II Frontiers in Genetics next generation sequencing rare diseases diagnosis whole-exome sequencing whole-genome sequencing copy number variants (CNV) sequencing |
| title | Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II |
| title_full | Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II |
| title_fullStr | Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II |
| title_full_unstemmed | Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II |
| title_short | Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II |
| title_sort | editorial next generation sequencing ngs for rare diseases diagnosis volume ii |
| topic | next generation sequencing rare diseases diagnosis whole-exome sequencing whole-genome sequencing copy number variants (CNV) sequencing |
| url | https://www.frontiersin.org/articles/10.3389/fgene.2023.1249585/full |
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