ArticleBMC bioinformatics2007
Effective selection of informative SNPs and classification on the HapMap genotype data.
Article in BMC bioinformatics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.
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Who cites it
16 citing papers in PubMed, 1 synthesis or guideline pooled it.
- New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals.Circulation. Cardiovascular genetics · 2017Pooled it
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- A single nucleotide polymorphism panel for individual identification and ancestry assignment in Caucasians and four East and Southeast Asian populations using a machine learning classifier.Forensic science, medicine, and pathology · 2019Article
- A Simple Algorithm for Population Classification.Scientific reports · 2016Article
- Discovering Alzheimer Genetic Biomarkers Using Bayesian Networks.Advances in bioinformatics · 2015Article
- Inferring population structure and relationship using minimal independent evolutionary markers in Y-chromosome: a hybrid approach of recursive feature selection for hierarchical clustering.Nucleic acids research · 2014Article
- Determination of sample size for a multi-class classifier based on single-nucleotide polymorphisms: a volume under the surface approach.BMC bioinformatics · 2014Article
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- Integrative analysis of single nucleotide polymorphisms and gene expression efficiently distinguishes samples from closely related ethnic populations.BMC genomics · 2012Article
- Psoriasis prediction from genome-wide SNP profiles.BMC dermatology · 2011Article
- Machine learning techniques for single nucleotide polymorphism--disease classification models in schizophrenia.Molecules (Basel, Switzerland) · 2010Article
- Identification of type 2 diabetes-associated combination of SNPs using support vector machine.BMC genetics · 2010Article
- Global haplotype partitioning for maximal associated SNP pairs.BMC bioinformatics · 2009Article
- A novel similarity-measure for the analysis of genetic data in complex phenotypes.BMC bioinformatics · 2009Article
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2 authors.
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Abstract
backgroundSince the single nucleotide polymorphisms (SNPs) are genetic variations which determine the difference between any two unrelated individuals, the SNPs can be used to identify the correct source population of an individual. For efficient population identification with the HapMap genotype data, as few informative SNPs as possible are required from the original 4 million SNPs. Recently, Park et al. (2006) adopted the nearest shrunken centroid method to classify the three populations, i.e., Utah residents with ancestry from Northern and Western Europe (CEU), Yoruba in Ibadan, Nigeria in West Africa (YRI), and Han Chinese in Beijing together with Japanese in Tokyo (CHB+JPT), from which 100,736 SNPs were obtained and the top 82 SNPs could completely classify the three populations.
resultsIn this paper, we propose to first rank each feature (SNP) using a ranking measure, i.e., a modified t-test or F-statistics. Then from the ranking list, we form different feature subsets by sequentially choosing different numbers of features (e.g., 1, 2, 3, ..., 100.) with top ranking values, train and test them by a classifier, e.g., the support vector machine (SVM), thereby finding one subset which has the highest classification accuracy. Compared to the classification method of Park et al., we obtain a better result, i.e., good classification of the 3 populations using on average 64 SNPs.
conclusionExperimental results show that the both of the modified t-test and F-statistics method are very effective in ranking SNPs about their classification capabilities. Combined with the SVM classifier, a desirable feature subset (with the minimum size and most informativeness) can be quickly found in the greedy manner after ranking all SNPs. Our method is able to identify a very small number of important SNPs that can determine the populations of individuals.
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