A computational method for genotype calling in family-based sequencing data.

Chang LC, Li B, Fang Z, Vrieze S, McGue M, Iacono WG, Tseng GC, Chen W
BMC Bioinformatics. 2016 17: 37

PMID: 26772743 · PMCID: PMC4715317 · DOI:10.1186/s12859-016-0880-5

BACKGROUND - As sequencing technologies can help researchers detect common and rare variants across the human genome in many individuals, it is known that jointly calling genotypes across multiple individuals based on linkage disequilibrium (LD) can facilitate the analysis of low to modest coverage sequence data. However, genotype-calling methods for family-based sequence data, particularly for complex families beyond parent-offspring trios, are still lacking.

RESULTS - In this study, first, we proposed an algorithm that considers both linkage disequilibrium (LD) patterns and familial transmission in nuclear and multi-generational families while retaining the computational efficiency. Second, we extended our method to incorporate external reference panels to analyze family-based sequence data with a small sample size. In simulation studies, we show that modeling multiple offspring can dramatically increase genotype calling accuracy and reduce phasing and Mendelian errors, especially at low to modest coverage. In addition, we show that using external panels can greatly facilitate genotype calling of sequencing data with a small number of individuals. We applied our method to a whole genome sequencing study of 1339 individuals at ~10X coverage from the Minnesota Center for Twin and Family Research.

CONCLUSIONS - The aggregated results show that our methods significantly outperform existing ones that ignore family constraints or LD information. We anticipate that our method will be useful for many ongoing family-based sequencing projects. We have implemented our methods efficiently in a C++ program FamLDCaller, which is available from http://www.pitt.edu/~wec47/famldcaller.html.

MeSH Terms (11)

Algorithms Computational Biology Computer Simulation Databases, Genetic Genome, Human Genotyping Techniques Haplotypes Humans Linkage Disequilibrium Polymorphism, Single Nucleotide Sequence Analysis, DNA

Connections (1)

This publication is referenced by other Labnodes entities:

Links