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A simple approach to rapidly process long-read NGS raw data into high-quality DNA sequences

1- UPLOAD YOUR RAW DATA

2- UPLOAD YOUR REFERENCE SEQUENCE

3- UPLOAD THE FASTA FILES OF RAW SUBREADS

4- LAUNCH YOUR ANALYSIS

Derive accurate variant calling from any gene in the human genome in only a few clicks

OUR WGS APPLICATION IS A CENTRALIZED PLATFORM THAT LET YOU ACCESS RAW DATA FROM YOUR OWN DATABASES AND RAPIDLY PROCESS IT TO EXTRACT HIGH QUALITY DNA SEQUENCES FROM ANY REGION IN THE HUMAN GENOME

A fully automated analytical approach

MINIMIZE THE TIME SPEND ON VARIANT CALLING AND GET HAPLOTYPE-RESOLVED VARIANTS MINUTES AFTER UPLOADING YOUR RAW DATA

GO STRAIGHT INTO DOWNSTREAM ANALYTICS AND SPEED UP DISCOVERY

THE AUTOMATED ANALYTICAL PLATFORM FOR LONG-READ NEXT GENERATION SEQUENCING