Cargando…
ClinVar data parsing
This software repository provides a pipeline for converting raw ClinVar data files into analysis-friendly tab-delimited tables, and also provides these tables for the most recent ClinVar release. Separate tables are generated for genome builds GRCh37 and GRCh38 as well as for mono-allelic variants a...
Autores principales: | Zhang, Xiaolei, Minikel, Eric V., O'Donnell-Luria, Anne H., MacArthur, Daniel G., Ware, James S., Weisburd, Ben |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473414/ https://www.ncbi.nlm.nih.gov/pubmed/28630944 http://dx.doi.org/10.12688/wellcomeopenres.11640.1 |
Ejemplares similares
-
Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts
por: Butler III, Robert R., et al.
Publicado: (2018) -
Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar database
por: Pérez-Palma, Eduardo, et al.
Publicado: (2019) -
Is ‘likely pathogenic’ really 90% likely? Reclassification data in ClinVar
por: Harrison, Steven M., et al.
Publicado: (2019) -
ClinVar: public archive of interpretations of clinically relevant variants
por: Landrum, Melissa J., et al.
Publicado: (2016) -
ClinVar: improving access to variant interpretations and supporting evidence
por: Landrum, Melissa J, et al.
Publicado: (2018)