MFEprimer Web Server 4.4.0

Since its launch in 2009, the MFEprimer Web Server has been in continuous operation for 17 years. We remain committed to maintaining this platform as a sustainable, long-term resource for the global research community.

Beginning with version 4.0, the server has evolved into a comprehensive platform for PCR primer quality assessment and design. Recently, we introduced Human pan-genome primer check for evaluating a primer pair across HPRC assemblies, alongside MP-Ref for multiplex design on reference genomes and MP-Methy for methylation primer design. A detailed overview of the available tools is provided below.

Quality Control Tools

  • Human pan-genome primer check New: Checks whether one primer pair amplifies across 97 human pan-genome assemblies (HPRC) and reports per-assembly coverage.
  • Specificity Check: Verifies primer specificity against multiple background databases to minimize off-target amplification.
  • Dimer Check: Evaluates the potential formation of primer–dimer structures that could compromise PCR performance.
  • Hairpin Check: Assesses the likelihood of hairpin structures that may reduce amplification efficiency.
  • Coverage Analysis for Microbes: Examines primer coverage across microbial strains to identify potential performance issues.

Primer Design Tools

  • MP-Ref: Multiplex PCR primer design for reference genomes. This enhanced tool supports a broad range of applications and streamlines primer design for complex multiplex PCR experiments.
  • MP-Methy: Multiplex primer design for bisulfite sequencing and methylation-specific PCR, facilitating research in DNA methylation and epigenetics.

Miscellaneous Tools

  • SubSeq: Enables retrieval of subsequences from FASTA databases for downstream analyses such as BLAST searches and GC-content evaluation.

History

  • 2019, MFEprimer-3.0: quality control for PCR primers.
  • 2012, MFEprimer-2.0: a fast thermodynamics-based program for checking PCR primer specificity.
  • 2009, MFEprimer-1.0: multiple factor evaluation of the specificity of PCR primers.