Evaluating variants classified as pathogenic in ClinVar in the DDD Study

PURPOSE: Automated variant filtering is an essential part of diagnostic genome-wide sequencing but may generate false negative results. We sought to investigate whether some previously identified pathogenic variants may be being routinely excluded by standard variant filtering pipelines. METHODS: We...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Genet Med
Prif Awduron: Wright, Caroline F., Eberhardt, Ruth Y., Constantinou, Panayiotis, Hurles, Matthew E., FitzPatrick, David R., Firth, Helen V.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group US 2020
Pynciau:
Brief Communication
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7935711/
https://ncbi.nlm.nih.gov/pubmed/33149276
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-020-01021-9
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