Cargando…
iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers
Accurate prediction of the pathogenicity of genomic variants, especially nonsynonymous single nucleotide variants (nsSNVs), is essential in biomedical research and clinical genetics. Most current prediction methods build a generic classifier for all genes. However, different genes and gene families...
Autores principales: | Wang, Meng, Wei, Liping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985647/ https://www.ncbi.nlm.nih.gov/pubmed/27527004 http://dx.doi.org/10.1038/srep31321 |
Ejemplares similares
-
Integrated EpCAM-independent subtraction enrichment and iFISH strategies to detect and classify disseminated and circulating tumors cells
por: Lin, Peter Ping
Publicado: (2015) -
Erratum to: Integrated EpCAM-independent subtraction enrichment and iFISH strategies to detect and classify disseminated and circulating tumors cells
por: Lin, Peter Ping
Publicado: (2016) -
iFISH is a publically available resource enabling versatile DNA FISH to study genome architecture
por: Gelali, Eleni, et al.
Publicado: (2019) -
The Utilization of Karyotyping, iFISH, and MLPA for the Detection of Recurrence Genetic Aberrations in Multiple Myeloma
por: Sommaluan, Suchada, et al.
Publicado: (2017) -
Comparison of analytic performances of Cellsearch and iFISH approach in detecting circulating tumor cells
por: Sheng, Yuan, et al.
Publicado: (2015)