P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S294977442400637X |
| _version_ | 1827321944472551424 |
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| author | Jaime Lopes Marcus Cannon Jonathan Turner Monica Roberts Theodore Markulin Christopher Fraher Bryan Killinger Stela Filipovic-Sadic Bradley Hall |
| author_facet | Jaime Lopes Marcus Cannon Jonathan Turner Monica Roberts Theodore Markulin Christopher Fraher Bryan Killinger Stela Filipovic-Sadic Bradley Hall |
| author_sort | Jaime Lopes |
| collection | DOAJ |
| first_indexed | 2024-04-25T01:16:53Z |
| format | Article |
| id | doaj.art-5d048ee931c941dcb31aa57535cf78c4 |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2024-04-25T01:16:53Z |
| publishDate | 2024-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-5d048ee931c941dcb31aa57535cf78c42024-03-09T09:32:48ZengElsevierGenetics in Medicine Open2949-77442024-01-012101491P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samplesJaime Lopes0Marcus Cannon1Jonathan Turner2Monica Roberts3Theodore Markulin4Christopher Fraher5Bryan Killinger6Stela Filipovic-Sadic7Bradley Hall8Cincinnati Children's Hospital Medical CenterCincinnati Children's Hospital Medical CenterAsuragen, a Bio-Techne BrandAsuragen, a Bio-Techne BrandAsuragen, a Bio-Techne BrandAsuragen, a Bio-Techne BrandAsuragen, a Bio-Techne BrandAsuragen, a Bio-Techne BrandAsuragen, a Bio-Techne Brandhttp://www.sciencedirect.com/science/article/pii/S294977442400637X |
| spellingShingle | Jaime Lopes Marcus Cannon Jonathan Turner Monica Roberts Theodore Markulin Christopher Fraher Bryan Killinger Stela Filipovic-Sadic Bradley Hall P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples Genetics in Medicine Open |
| title | P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples |
| title_full | P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples |
| title_fullStr | P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples |
| title_full_unstemmed | P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples |
| title_short | P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples |
| title_sort | p585 amplification based nanopore sequencing accurately detects hba and hbb snvs indels and structural variants in clinical thalassemia samples |
| url | http://www.sciencedirect.com/science/article/pii/S294977442400637X |
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