Title
In silico phenotyping via co-training for improved phenotype prediction from genotype
Abstract
Motivation: Predicting disease phenotypes from genotypes is a key challenge in medical applications in the postgenomic era. Large training datasets of patients that have been both genotyped and phenotyped are the key requisite when aiming for high prediction accuracy. With current genotyping projects producing genetic data for hundreds of thousands of patients, large-scale phenotyping has become the bottleneck in disease phenotype prediction. Results: Here we present an approach for imputing missing disease phenotypes given the genotype of a patient. Our approach is based on co-training, which predicts the phenotype of unlabeled patients based on a second class of information, e.g. clinical health record information. Augmenting training datasets by this type of in silico phenotyping can lead to significant improvements in prediction accuracy. We demonstrate this on a dataset of patients with two diagnostic types of migraine, termed migraine with aura and migraine without aura, from the International Headache Genetics Consortium. Conclusions: Imputing missing disease phenotypes for patients via co-training leads to larger training datasets and improved prediction accuracy in phenotype prediction.
Year
DOI
Venue
2015
10.1093/bioinformatics/btv254
BIOINFORMATICS
Field
DocType
Volume
Data mining,Genotype,Migraine with aura,Disease,Genotyping,Phenotype,Computer science,Co-training,Bioinformatics,Genotyping Techniques,In silico
Journal
31
Issue
ISSN
Citations 
12
1367-4803
1
PageRank 
References 
Authors
0.35
6
6