Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders
Background: Both whole exome sequencing and copy number variants sequencing were applied to identify the genetic cause of rare pediatric disorders. In our study, we aimed to investigate the diagnostic yield of parallel tests of trio whole exome sequencing and copy number variants sequencing and its...
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2020-06-01
|
| Series: | Frontiers in Genetics |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/article/10.3389/fgene.2020.00473/full |
| id |
doaj-1ed0b1ec718b4ac2a26afa3be9f800b3 |
|---|---|
| record_format |
Article |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
Xuyun Hu Xuyun Hu Xuyun Hu Ruolan Guo Ruolan Guo Ruolan Guo Jun Guo Jun Guo Jun Guo Zhan Qi Zhan Qi Zhan Qi Wei Li Wei Li Wei Li Chanjuan Hao Chanjuan Hao Chanjuan Hao |
| spellingShingle |
Xuyun Hu Xuyun Hu Xuyun Hu Ruolan Guo Ruolan Guo Ruolan Guo Jun Guo Jun Guo Jun Guo Zhan Qi Zhan Qi Zhan Qi Wei Li Wei Li Wei Li Chanjuan Hao Chanjuan Hao Chanjuan Hao Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders Frontiers in Genetics whole exome sequencing copy number variants sequencing pediatric disorders cost-effective clinical utility |
| author_facet |
Xuyun Hu Xuyun Hu Xuyun Hu Ruolan Guo Ruolan Guo Ruolan Guo Jun Guo Jun Guo Jun Guo Zhan Qi Zhan Qi Zhan Qi Wei Li Wei Li Wei Li Chanjuan Hao Chanjuan Hao Chanjuan Hao |
| author_sort |
Xuyun Hu |
| title |
Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders |
| title_short |
Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders |
| title_full |
Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders |
| title_fullStr |
Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders |
| title_full_unstemmed |
Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders |
| title_sort |
parallel tests of whole exome sequencing and copy number variant sequencing increase the diagnosis yields of rare pediatric disorders |
| publisher |
Frontiers Media S.A. |
| series |
Frontiers in Genetics |
| issn |
1664-8021 |
| publishDate |
2020-06-01 |
| description |
Background: Both whole exome sequencing and copy number variants sequencing were applied to identify the genetic cause of rare pediatric disorders. In our study, we aimed to investigate the diagnostic yield of parallel tests of trio whole exome sequencing and copy number variants sequencing and its clinical utility.Methods: After collecting detailed clinical information, a total of 60 patients were referred to parallel tests of whole exome sequencing and copy number variants sequencing, which used shared initial libraries.Results: 26 pathogenic or likely pathogenic single nucleotide variants and 11 copy number variants were identified in 32 patients. 65.4% (17/26) of the SNVs were novel. The overall diagnosis rate was 53.3%. For the patients with positive results, 22 (36.7%) patients were diagnosed by whole exome sequencing and 10 (16.7%) patients were diagnosed by copy number variants sequencing. We also reviewed clinical impact on selected cases.Conclusion: We adopted an approach by performing parallel tests of trio whole exome sequencing and copy number variants sequencing with shared initial libraries. This strategy is relatively efficient and cost-effective for the diagnosis of rare pediatric disorders with high heterogeneity. |
| topic |
whole exome sequencing copy number variants sequencing pediatric disorders cost-effective clinical utility |
| url |
https://www.frontiersin.org/article/10.3389/fgene.2020.00473/full |
| work_keys_str_mv |
AT xuyunhu paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT xuyunhu paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT xuyunhu paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT ruolanguo paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT ruolanguo paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT ruolanguo paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT junguo paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT junguo paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT junguo paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT zhanqi paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT zhanqi paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT zhanqi paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT weili paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT weili paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT weili paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT chanjuanhao paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT chanjuanhao paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders AT chanjuanhao paralleltestsofwholeexomesequencingandcopynumbervariantsequencingincreasethediagnosisyieldsofrarepediatricdisorders |
| _version_ |
1724747725151404032 |
| spelling |
doaj-1ed0b1ec718b4ac2a26afa3be9f800b32020-11-25T02:48:27ZengFrontiers Media S.A.Frontiers in Genetics1664-80212020-06-011110.3389/fgene.2020.00473527584Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric DisordersXuyun Hu0Xuyun Hu1Xuyun Hu2Ruolan Guo3Ruolan Guo4Ruolan Guo5Jun Guo6Jun Guo7Jun Guo8Zhan Qi9Zhan Qi10Zhan Qi11Wei Li12Wei Li13Wei Li14Chanjuan Hao15Chanjuan Hao16Chanjuan Hao17Beijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaMOE Key Laboratory of Major Diseases in Children, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaHenan Key Laboratory of Pediatric Inherited & Metabolic Diseases, Henan Children's Hospital, Zhengzhou Hospital of Beijing Children's Hospital, Zhengzhou, ChinaBeijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaMOE Key Laboratory of Major Diseases in Children, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaHenan Key Laboratory of Pediatric Inherited & Metabolic Diseases, Henan Children's Hospital, Zhengzhou Hospital of Beijing Children's Hospital, Zhengzhou, ChinaBeijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaMOE Key Laboratory of Major Diseases in Children, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaHenan Key Laboratory of Pediatric Inherited & Metabolic Diseases, Henan Children's Hospital, Zhengzhou Hospital of Beijing Children's Hospital, Zhengzhou, ChinaBeijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaMOE Key Laboratory of Major Diseases in Children, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaHenan Key Laboratory of Pediatric Inherited & Metabolic Diseases, Henan Children's Hospital, Zhengzhou Hospital of Beijing Children's Hospital, Zhengzhou, ChinaBeijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaMOE Key Laboratory of Major Diseases in Children, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaHenan Key Laboratory of Pediatric Inherited & Metabolic Diseases, Henan Children's Hospital, Zhengzhou Hospital of Beijing Children's Hospital, Zhengzhou, ChinaBeijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaMOE Key Laboratory of Major Diseases in Children, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, ChinaHenan Key Laboratory of Pediatric Inherited & Metabolic Diseases, Henan Children's Hospital, Zhengzhou Hospital of Beijing Children's Hospital, Zhengzhou, ChinaBackground: Both whole exome sequencing and copy number variants sequencing were applied to identify the genetic cause of rare pediatric disorders. In our study, we aimed to investigate the diagnostic yield of parallel tests of trio whole exome sequencing and copy number variants sequencing and its clinical utility.Methods: After collecting detailed clinical information, a total of 60 patients were referred to parallel tests of whole exome sequencing and copy number variants sequencing, which used shared initial libraries.Results: 26 pathogenic or likely pathogenic single nucleotide variants and 11 copy number variants were identified in 32 patients. 65.4% (17/26) of the SNVs were novel. The overall diagnosis rate was 53.3%. For the patients with positive results, 22 (36.7%) patients were diagnosed by whole exome sequencing and 10 (16.7%) patients were diagnosed by copy number variants sequencing. We also reviewed clinical impact on selected cases.Conclusion: We adopted an approach by performing parallel tests of trio whole exome sequencing and copy number variants sequencing with shared initial libraries. This strategy is relatively efficient and cost-effective for the diagnosis of rare pediatric disorders with high heterogeneity.https://www.frontiersin.org/article/10.3389/fgene.2020.00473/fullwhole exome sequencingcopy number variants sequencingpediatric disorderscost-effectiveclinical utility |