Whole GenomeL - Long Reads Whole Genome Sequencing
Whole GenomeL - based on Third-generation sequencing (also known as long-read sequencing). The first Long Reads Whole Genome Sequencing available commercially, worldwide. Leveraging Third-generation sequencing technology in the Dante Labs Oxford Nanopore-certified lab
To get a Genomic Snapshot of what you are most interested in, please fill out this form after receiving your saliva collection kit
What you get
Long Read Raw Data
Download your FASTQ, BAM and VCF files, with no extra charge.
CNV and SV
Leverage long reads for Copy Number Variations and Structural Variations
LONG READS
Leverage Third Generation Sequencing to receive data on your entire DNA based on long reads by Oxford Nanopore
Long reads Whole Genome Sequencing:
- - Read length: average N50>20,000bp (vs. 150bp of short reads)
- - Optimized for analysis of repeated sequences, copy number variations and structural variations
- - Third generation sequencing
- - First time available, global coverage
- - Performed at Dante Labs own Oxford Nanopore-certified sequencing center
How it works
Purchase Your Kit Online
Your kit will arrive in 2-3 Business days.
Collect and Register
Follow the kit instructions to spit in the tube - all from home. Register your kit on our website and then mail the saliva sample tube back to us.
Get your Full Raw Data online
In about 8-10 weeks, we will send you an email to let you know that we completed your analysis.