Sharing genetic variants with the NGS pipeline is essential for effective genomic data sharing and reproducibility in health information exchange
Abstract Genetic variants causing underlying pharmacogenetic and disease phenotypes have been used as the basis for clinical decision-making. However, due to the lack of standards for next-generation sequencing (NGS) pipelines, reproducing genetic variants among institutions is still difficult. The...
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| Auteurs principaux: | , , |
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| Format: | article |
| Langue: | EN |
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Nature Portfolio
2021
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| Accès en ligne: | https://doaj.org/article/b026acb47b924d8a853c52553e34ffb5 |
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