Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population

BMC Genomics. 2014 Aug 10;15(1):673. doi: 10.1186/1471-2164-15-673.

Abstract

Background: Validation of single nucleotide variations in whole-genome sequencing is critical for studying disease-related variations in large populations. A combination of different types of next-generation sequencers for analyzing individual genomes may be an efficient means of validating multiple single nucleotide variations calls simultaneously.

Results: Here, we analyzed 12 independent Japanese genomes using two next-generation sequencing platforms: the Illumina HiSeq 2500 platform for whole-genome sequencing (average depth 32.4×), and the Ion Proton semiconductor sequencer for whole exome sequencing (average depth 109×). Single nucleotide polymorphism (SNP) calls based on the Illumina Human Omni 2.5-8 SNP chip data were used as the reference. We compared the variant calls for the 12 samples, and found that the concordance between the two next-generation sequencing platforms varied between 83% and 97%.

Conclusions: Our results show the versatility and usefulness of the combination of exome sequencing with whole-genome sequencing in studies of human population genetics and demonstrate that combining data from multiple sequencing platforms is an efficient approach to validate and supplement SNP calls.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Composition
  • Exome / genetics*
  • Female
  • Genome, Human / genetics
  • Genomics / instrumentation*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Male
  • Polymorphism, Single Nucleotide*
  • Reproducibility of Results
  • Semiconductors*
  • Sequence Analysis, DNA / instrumentation*