P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive care
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2023-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774423004843 |
| _version_ | 1827242944897220608 |
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| author | Jonathan Cayouette Philippe Thibault Jacques Michaud Sebastien Levesque |
| author_facet | Jonathan Cayouette Philippe Thibault Jacques Michaud Sebastien Levesque |
| author_sort | Jonathan Cayouette |
| collection | DOAJ |
| first_indexed | 2024-03-08T10:26:18Z |
| format | Article |
| id | doaj.art-1b0c2df1a5324022b743e2b664171d05 |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2025-03-21T22:04:26Z |
| publishDate | 2023-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-1b0c2df1a5324022b743e2b664171d052024-05-25T04:58:05ZengElsevierGenetics in Medicine Open2949-77442023-01-0111100484P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive careJonathan Cayouette0Philippe Thibault1Jacques Michaud2Sebastien Levesque3Medical Genetics Service, Department of Pediatrics, Faculty of Medicine and Health Sciences, University of SherbrookeMedical Genetics Service, Department of Pediatrics, Faculty of Medicine and Health Sciences, University of SherbrookeDepartment of Neurosciences and Department of Pediatrics, Faculty of Medicine, University of MontrealMedical Genetics Service, Department of Pediatrics, Faculty of Medicine and Health Sciences, University of Sherbrookehttp://www.sciencedirect.com/science/article/pii/S2949774423004843 |
| spellingShingle | Jonathan Cayouette Philippe Thibault Jacques Michaud Sebastien Levesque P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive care Genetics in Medicine Open |
| title | P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive care |
| title_full | P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive care |
| title_fullStr | P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive care |
| title_full_unstemmed | P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive care |
| title_short | P437: Optimization of the diagnostic aid PhenoVar for the interpretation of rapid whole genome sequencing data in newborns in intensive care |
| title_sort | p437 optimization of the diagnostic aid phenovar for the interpretation of rapid whole genome sequencing data in newborns in intensive care |
| url | http://www.sciencedirect.com/science/article/pii/S2949774423004843 |
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