Cargando…
BBGRE: brain and body genetic resource exchange
Studies of copy number variation (genomic imbalance) are providing insight into both complex and Mendelian genetic disorders. Array comparative genomic hybridization (array CGH), a tool for detecting copy number variants at a resolution previously unattainable in clinical diagnostics, is increasingl...
Autores principales: | Ahn, Joo Wook, Dixit, Abhishek, Johnston, Caroline, Ogilvie, Caroline M., Collier, David A., Curran, Sarah, Dobson, Richard J. B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3785255/ https://www.ncbi.nlm.nih.gov/pubmed/24077841 http://dx.doi.org/10.1093/database/bat067 |
Ejemplares similares
-
SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes
por: Hariprakash, Judith Mary, et al.
Publicado: (2018) -
GESDB: a platform of simulation resources for genetic epidemiology studies
por: Yao, Po-Ju, et al.
Publicado: (2016) -
HGV&TB: a comprehensive online resource on human genes and genetic variants associated with tuberculosis
por: Sahajpal, Ruchika, et al.
Publicado: (2014) -
MGIS: managing banana (Musa spp.) genetic resources information and high-throughput genotyping data
por: Ruas, Max, et al.
Publicado: (2017) -
ParaPep: a web resource for experimentally validated antiparasitic peptide sequences and their structures
por: Mehta, Divya, et al.
Publicado: (2014)