Finding new structural and sequence attributes to predict possible disease association of single amino acid polymorphism (SAP)
Author(s) -
Zhiqiang Ye,
Shuqi Zhao,
Ge Gao,
Xiao Liu,
Robert Langlois,
Hui Lü,
Liping Wei
Publication year - 2007
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btm119
Subject(s) - web server , classifier (uml) , support vector machine , computational biology , computer science , single nucleotide polymorphism , web site , data mining , genetic association , biology , machine learning , artificial intelligence , bioinformatics , genetics , the internet , genotype , gene , world wide web
The rapid accumulation of single amino acid polymorphisms (SAPs), also known as non-synonymous single nucleotide polymorphisms (nsSNPs), brings the opportunities and needs to understand and predict their disease association. Currently published attributes are limited, the detailed mechanisms governing the disease association of a SAP remain unclear and thus, further investigation of new attributes and improvement of the prediction are desired.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom