Cargando…
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
HbVar (http://globin.bx.psu.edu/hbvar) is a widely-used locus-specific database (LSDB) launched 20 years ago by a multi-center academic effort to provide timely information on the numerous genomic variants leading to hemoglobin variants and all types of thalassemia and hemoglobinopathies. Here, we r...
Autores principales: | Giardine, Belinda M, Joly, Philippe, Pissard, Serge, Wajcman, Henri, K. Chui, David H, Hardison, Ross C, Patrinos, George P |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778921/ https://www.ncbi.nlm.nih.gov/pubmed/33125055 http://dx.doi.org/10.1093/nar/gkaa959 |
Ejemplares similares
-
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
por: Giardine, Belinda, et al.
Publicado: (2014) -
ClinVar: public archive of interpretations of clinically relevant variants
por: Landrum, Melissa J., et al.
Publicado: (2016) -
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies
por: Viennas, Emmanouil, et al.
Publicado: (2017) -
RiceVarMap: a comprehensive database of rice genomic variations
por: Zhao, Hu, et al.
Publicado: (2014) -
rVarBase: an updated database for regulatory features of human variants
por: Guo, Liyuan, et al.
Publicado: (2016)