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Sharing genetic variants with the NGS pipeline is essential for effective genomic data sharing and reproducibility in health information exchange
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 aim of th...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Nature Publishing Group UK
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838410/ https://www.ncbi.nlm.nih.gov/pubmed/33500538 http://dx.doi.org/10.1038/s41598-021-82006-9 |