Molecular Diagnostics & PCR Assay Design
We design robust PCR primers and probe-based assays for research and diagnostic workflows from singleplex tests to high-plex panels prioritizing specificity, reproducibility, and clear deliverables.
Typical outputs
- Primer/probe sequences + Tm/GC/amplicon size
- Specificity & off-target report
- Multiplex compatibility checks
- Ready-to-order table (CSV/Excel)
What we develop
PCR primers
Endpoint PCR and genotyping assays optimized for efficiency, specificity, and clean amplification.
qPCR / probe assays
Hydrolysis or hybridization probe sets, with attention to SNP/indel positioning and assay stability.
Multiplex & high-plex panels
Panel construction and balancing strategies for dozens to hundreds of targets (tiling or gene panels).
Polymorphism detection
Assays for discriminating individuals, lines, or populations using SNPs/indels and repeat-associated loci.
Where PCR diagnostics are applied
- Pathogen detection and strain/variant screening
- Genetic disorder testing and carrier screening (research use)
- Paternity/kinship and identity testing (where permitted)
- Forensics and criminal investigation support workflows
- Polymorphism and marker-assisted selection in plants/animals
- Site-directed mutagenesis and clone validation
- Validation of sequencing or microarray findings
- Targeted amplicon sequencing preparation (Illumina/ONT)
Quality controls we emphasize
How the workflow typically runs
Inputs
Targets (FASTA), coordinates, or gene lists; organism/build; constraints (amplicon length, chemistry).
Design
Candidate primer/probe generation with thermodynamic constraints and repeat-aware filtering.
In-silico validation
Mapping/off-target checks, amplicon verification, and multiplex interaction scanning.
Deliverables
Final assay table and reports; optional pooling guidance for high-plex panels.
Discuss your diagnostic project
Share target sequences, organism/build, and assay type. We will propose an efficient design strategy and deliverables.