One standard for all labs and projects.
spcfy turns raw sequencing runs into standardized, comparable results for everyone that generate biodiversity data: laboratories that run the wet-lab and sequencing side, and bioinformaticians who process, validate, and interpret the results.
Working across both? Many labs run bioinformatics in-house, and many bioinformaticians work inside a lab rather than alongside one. spcfy connects the same standardized pipeline either way, whichever role describes your work today.
Tailored eDNA & metabarcoding solutions for laboratories
spcfy handles the full bioinformatics workflow from raw FASTQ files to finished reports, so your lab can focus on generating insights instead of maintaining pipelines. Scalable analysis and consistent accuracy come built in.
Less pipeline maintenance, more consistent delivery.
Convert raw FASTQ files into standardized reports with minimal manual effort.
Access curated, regularly updated databases across animals, fungi, bacteria, and plants.
Analyze species communities across multiple taxa with consistent precision.
Handle sequencing runs of any size with flexible computing power on demand.
Skip the pipeline plumbing. Keep every parameter visible.
spcfy bridges raw sequencing data and high level analysis with standardized workflows and curated reference databases, removing the burden of pipeline maintenance and manual cleanup so you can focus on interpretation.
Less pipeline upkeep, more room for interpretation.
Standardized workflows for 16S, 12S, CO1, and ITS2, without manual script maintenance.
Access up to date reference libraries: NCBI, SILVA, BOLD, and UNITE.
Keep long term data consistent through unified OTU parameters across all projects.
Link wetlab metadata to results with full transparency on read counts and filtering.