Cargando…
Locus Reference Genomic sequences: an improved basis for describing human DNA variants
As our knowledge of the complexity of gene architecture grows, and we increase our understanding of the subtleties of gene expression, the process of accurately describing disease-causing gene variants has become increasingly problematic. In part, this is due to current reference DNA sequence format...
Autores principales: | Dalgleish, Raymond, Flicek, Paul, Cunningham, Fiona, Astashyn, Alex, Tully, Raymond E, Proctor, Glenn, Chen, Yuan, McLaren, William M, Larsson, Pontus, Vaughan, Brendan W, Béroud, Christophe, Dobson, Glen, Lehväslaiho, Heikki, Taschner, Peter EM, den Dunnen, Johan T, Devereau, Andrew, Birney, Ewan, Brookes, Anthony J, Maglott, Donna R |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873802/ https://www.ncbi.nlm.nih.gov/pubmed/20398331 http://dx.doi.org/10.1186/gm145 |
Ejemplares similares
-
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants
por: MacArthur, Jacqueline A. L., et al.
Publicado: (2014) -
VarioML framework for comprehensive variation data representation and exchange
por: Byrne, Myles, et al.
Publicado: (2012) -
A database and API for variation, dense genotyping and resequencing data
por: Rios, Daniel, et al.
Publicado: (2010) -
Considerations for the inclusion of 2x mammalian genomes in phylogenetic analyses
por: Vilella, Albert J, et al.
Publicado: (2011) -
Ensembl variation resources
por: Chen, Yuan, et al.
Publicado: (2010)