The science

How DNA barcoding works

DNA barcoding uses short, standardised genetic markers to identify organisms to species level. Just as a supermarket barcode identifies a product, a DNA barcode identifies a species. Here's the process.

You collect a sample

A tiny piece of tissue (~5mm) goes into a tube with ethanol preservative. For fungi, we recommend inner stipe tissue to avoid surface contaminants. Photograph the specimen first — morphology helps confirm the molecular ID.

DNA extraction

We break open cells using our Extract-N-Amp protocol — a fast alkaline lysis that releases DNA from the tissue. The extracted DNA is diluted and ready for amplification.

PCR amplification

Using specific primers (e.g. ITS1-F and ITS4 for fungi), we make billions of copies of the barcode region via PCR. A gel electrophoresis check confirms we got a clean product.

Sanger sequencing

The amplified DNA is sent to AGRF for Sanger sequencing. Fluorescent dye terminators generate a chromatogram — the raw signal that becomes your DNA sequence.

Bioinformatics

We trim low-quality ends, assemble forward and reverse reads, then BLAST against curated databases (UNITE for fungi, GenBank, BOLD) to find the closest matching species.

Your report

You receive a detailed HTML report with species identification, confidence level, chromatogram trace, phylogenetic tree, BLAST hits, and the story behind your organism.