Cargando…
nsSNPAnalyzer: identifying disease-associated nonsynonymous single nucleotide polymorphisms
Nonsynonymous single nucleotide polymorphisms (nsSNPs) are prevalent in genomes and are closely associated with inherited diseases. To facilitate identifying disease-associated nsSNPs from a large number of neutral nsSNPs, it is important to develop computational tools to predict the nsSNP's ph...
Autores principales: | Bao, Lei, Zhou, Mi, Cui, Yan |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1160133/ https://www.ncbi.nlm.nih.gov/pubmed/15980516 http://dx.doi.org/10.1093/nar/gki372 |
Ejemplares similares
-
SNPAnalyzer: a web-based integrated workbench for single-nucleotide polymorphism analysis
por: Yoo, Jinho, et al.
Publicado: (2005) -
Prediction of Deleterious Nonsynonymous Single-Nucleotide Polymorphism for Human Diseases
por: Wu, Jiaxin, et al.
Publicado: (2013) -
A Simulation Analysis and Screening of Deleterious Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Sheep LEP Gene
por: Girmay, Shishay, et al.
Publicado: (2022) -
Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity
por: Bouafi, Hind, et al.
Publicado: (2019) -
IDRMutPred: predicting disease-associated germline nonsynonymous single nucleotide variants (nsSNVs) in intrinsically disordered regions
por: Zhou, Jing-Bo, et al.
Publicado: (2020)