4.8 Article

MFEprimer-3.0: quality control for PCR primers

Journal

NUCLEIC ACIDS RESEARCH
Volume 47, Issue W1, Pages W610-W613

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkz351

Keywords

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Funding

  1. National Natural Science Foundation of China [U1603120, 31571314, 31771394]
  2. Research Foundation of iGeneTech [2016SX001, 2017SX003]

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Quality control (QC) for lab-designed primers is crucial for the success of a polymerase chain reaction (PCR). Here, we present MFEprimer-3.0, a functional primer quality control program for checking nonspecific amplicons, dimers, hairpins and other parameters. The new features of the current version include: (i) more sensitive binding site search using the updated k-mer algorithm that allows mismatches within the k-mer, except for the first base at the 3' end. The binding sites of each primer with a stable 3' end are listed in the output; (ii) new algorithms for rapidly identifying self-dimers, cross-dimers and hairpins; (iii) the command-line version, which has an added option of JSON output to enhance the versatility of MFEprimer by acting as a QC step in the 'primer design -> quality control -> redesign' pipeline; (iv) a function for checking whether the binding sites contain single nucleotide polymorphisms (SNPs), which will affect the consistency of binding efficiency among different samples. In summary, MFEprimer-3.0 is updated with the well-tested PCR primer QC program and it can be integrated into various PCR primer design applications as a QC module. The MFEprimer-3.0 server is freely accessible without any login requirement at: https://mfeprimer3.igenetech.com/ and https://www.mfeprimer.com/. The source code for the command-line version is a vailable upon request.

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