Region-based and pathway-based QTL mapping using a p-value combination method

BMC Proceedings

Proceedings

Hsin-Chou Yang¹  Chia-Wei Chen¹ 

[1] Institute of Statistical Science, Academia Sinica, Nankang 115, Taipei, Taiwan;

关键词: Quantitative Trait Locus;    Rare Variant;    Quantitative Trait Locus Mapping;    Common SNPs;    Vascular Endothelial Growth Factor Pathway;   

DOI  :  10.1186/1753-6561-5-S9-S43

来源: Springer

【 摘 要 】

Quantitative trait locus (QTL) mapping using deep DNA sequencing data is a challenging task. In this study we performed region-based and pathway-based QTL mappings using a p-value combination method to analyze the simulated quantitative traits Q1 and Q4 and the exome sequencing data. The aims were to evaluate the performance of the QTL mapping approaches that were used and to suggest plausible strategies for QTL mapping of DNA sequencing data. We conducted single-locus QTL mappings using a linear regression model with adjustments for age and smoking status, and we also conducted region-based and pathway-based QTL mappings using a truncated product method for combining p-values from the single-locus QTL mapping. To account for the features of rare variants and common single-nucleotide polymorphisms (SNPs), we considered independently rare-variant-only, common-SNP-only, and combined analyses. An analysis of 200 simulated replications showed that the three region-based methods reasonably controlled type I error, whereas the combined analysis yielded the greatest statistical power. Rare-variant-only, common-SNP-only, and combined analyses were also applied to pathway-based QTL mappings. We found that pathway-based QTL mappings had a power of approximately 100% when the significance of the vascular endothelial growth factor pathway was evaluated, but type I errors were slightly inflated. Our approach complements single-locus QTL mapping. An integrated approach using single-locus, combined region-based, and combined pathway-based analyses should yield promising results for QTL mapping of DNA sequencing data.

【 授权许可】

CC BY   
© Yang and Chen; licensee BioMed Central Ltd. 2011