Abstract

BackgroundPolymerase chain reaction (PCR) is used in directed sequencing for the discovery of novel polymorphisms. As the first step in PCR directed sequencing, effective PCR primer design is crucial for obtaining high-quality sequence data for target regions. Since current computational primer design tools are not fully tuned with stable underlying laboratory protocols, researchers may still be forced to iteratively optimize protocols for failed amplifications after the primers have been ordered. Furthermore, potentially identifiable factors which contribute to PCR failures have yet to be elucidated. This inefficient approach to primer design is further intensified in a high-throughput laboratory, where hundreds of genes may be targeted in one experiment.ResultsWe have developed a fully integrated computational PCR primer design pipeline that plays a key role in our high-throughput directed sequencing pipeline. Investigators may specify target regions defined through a rich set of descriptors, such as Ensembl accessions and arbitrary genomic coordinates. Primer pairs are then selected computationally to produce a minimal amplicon set capable of tiling across the specified target regions. As part of the tiling process, primer pairs are computationally screened to meet the criteria for success with one of two PCR amplification protocols. In the process of improving our sequencing success rate, which currently exceeds 95% for exons, we have discovered novel and accurate computational methods capable of identifying primers that may lead to PCR failures. We reveal the laboratory protocols and their associated, empirically determined computational parameters, as well as describe the novel computational methods which may benefit others in future primer design research.ConclusionThe high-throughput PCR primer design pipeline has been very successful in providing the basis for high-quality directed sequencing results and for minimizing costs associated with labor and reprocessing. The modular architecture of the primer design software has made it possible to readily integrate additional primer critique tests based on iterative feedback from the laboratory. As a result, the primer design software, coupled with the laboratory protocols, serves as a powerful tool for low and high-throughput primer design to enable successful directed sequencing.

Highlights

  • Polymerase chain reaction (PCR) is used in directed sequencing for the discovery of novel polymorphisms

  • JCVI projects #1 and #2 consisted of 121 genes where, for each gene, the regions targeted for primer design consisted of exons, intronic evolutionary conserved regions (ECRs) and 2 kbp upstream and downstream of the first and last exon, respectively

  • Since noncontiguous target regions are independent, primer pairs for each individual target region can be designed on separate processors

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Summary

Introduction

Polymerase chain reaction (PCR) is used in directed sequencing for the discovery of novel polymorphisms. Potentially identifiable factors which contribute to PCR failures have yet to be elucidated This inefficient approach to primer design is further intensified in a highthroughput laboratory, where hundreds of genes may be targeted in one experiment. Our primer design pipeline is further enhanced by a higher degree of operational automation and the parameterization of many key attributes in its design. We have employed this pipeline for over five years at our sequencing center and its use was instrumental in the publication of mutations discovered in a set of 20 tyrosine kinase receptor domains consisting of 160 exons, across 19 tumor samples in glioblastomas [9]. Our directed sequencing pipeline has achieved a sequencing success rate of over 90% (Table 3) and we have detected over 7200 potential variations in 150 genes, 3408 of which were not previously recorded in NCBI's dbSNP

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