Cargando…
Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts
Estimates from large scale genome sequencing studies indicate that each human carries up to 20 genetic variants that are predicted to results in loss of function (LOF) of protein-coding genes. While some are known disease-causing variants or common, tolerated, LOFs in non-essential genes, the majori...
Autores principales: | Sleiman, Patrick, Bradfield, Jonathan, Mentch, Frank, Almoguera, Berta, Connolly, John, Hakonarson, Hakon |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010747/ https://www.ncbi.nlm.nih.gov/pubmed/24808909 http://dx.doi.org/10.3389/fgene.2014.00105 |
Ejemplares similares
-
Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts
por: Connolly, John J., et al.
Publicado: (2014) -
Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes
por: Almoguera, Berta, et al.
Publicado: (2014) -
Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium
por: Qu, Hui-Qi, et al.
Publicado: (2022) -
HIF-1α Pulmonary Phenotype Wide Association Study Unveils a Link to Inflammatory Airway Conditions
por: Kelchtermans, Jelte, et al.
Publicado: (2021) -
COVID-19 in pediatrics: Genetic susceptibility
por: Glessner, Joseph T., et al.
Publicado: (2022)