AI Article Synopsis

  • Long-read sequencing technologies from PacBio and ONT allow for the phasing of mutations that are located several kilobases apart, which is important for understanding genetic variations.
  • The study utilized long-range PCR combined with ONT and PacBio sequencing to successfully phase two variants in the RET gene that are 9 kb apart and re-evaluated existing data on other important haplotypes.
  • The researchers identified potential methodological issues, such as PCR-chimera formation and reference alignment bias, that could compromise the accuracy of phasing variants using these advanced sequencing techniques.

Article Abstract

The long-read sequencers from Pacific Bioscience (PacBio) and Oxford Nanopore Technologies (ONT) offer the opportunity to phase mutations multiple kilobases apart directly from sequencing reads. In this study, we used long-range PCR with ONT and PacBio sequencing to phase two variants 9 kb apart in the RET gene. We also re-analysed data from a recent paper which had apparently successfully used ONT to phase clinically important haplotypes at the CYP2D6 and HLA loci. From these analyses, we demonstrate PCR-chimera formation during PCR amplification and reference alignment bias are pitfalls that need to be considered when attempting to phase variants using amplicon-based long-read sequencing technologies. These methodological pitfalls need to be avoided if the opportunities provided by long-read sequencers are to be fully exploited.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756330PMC
http://dx.doi.org/10.1038/srep21746DOI Listing

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