Comparison of Sequencing Platforms for Single Nucleotide Variant Calls in a Human Sample |
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| Authors: | Aakrosh Ratan Webb Miller Joseph Guillory Jeremy Stinson Somasekar Seshagiri Stephan C. Schuster |
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| Affiliation: | 1. Center for Comparative Genomics and Bioinformatics, Pennsylvania State University, University Park, Pennsylvania, United States of America.; 2. Department of Molecular Biology, Genentech Inc., South San Francisco, California, United States of America.; University of California, Irvine, United States of America, |
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| Abstract: | Next-generation sequencings platforms coupled with advanced bioinformatic tools enable re-sequencing of the human genome at high-speed and large cost savings. We compare sequencing platforms from Roche/454(GS FLX), Illumina/HiSeq (HiSeq 2000), and Life Technologies/SOLiD (SOLiD 3 ECC) for their ability to identify single nucleotide substitutions in whole genome sequences from the same human sample. We report on significant GC-related bias observed in the data sequenced on Illumina and SOLiD platforms. The differences in the variant calls were investigated with regards to coverage, and sequencing error. Some of the variants called by only one or two of the platforms were experimentally tested using mass spectrometry; a method that is independent of DNA sequencing. We establish several causes why variants remained unreported, specific to each platform. We report the indel called using the three sequencing technologies and from the obtained results we conclude that sequencing human genomes with more than a single platform and multiple libraries is beneficial when high level of accuracy is required. |
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