Our Technology
Long Read Nanopore Sequencing
Using the latest nanopore chemistry, we can accurately construct your sequence de novo or align to an optional reference. Detect indels or SNPs with high confidence.
Mail-In or Dropbox Samples
Set up your dropbox (Bay Area only) or mail-in your samples from anywhere. More details on our Dropbox and Shipping Info page.
Comprehensive reports - ALL INCLUDED!
Interactive Sequence Plot with Annotations
GenBank, GFF and FASTA files
AB1 file (align with your favorite tool like Benchling or SnapGene)
Read-length Histogram
Confidence report
Contamination report
Multimer report
Coverage plot
Save time and send us your colonies on a plate
Skip the miniprep. You can number the colonies if you want us to prep and sequence multiple isolates.
We can help explain your NGS data
Need to build a reference genome for your organism? Curious why your plasmid has unintended mutations? Unsure how to interpret the breseq report? Our PhD scientists will gladly answer any questions you might have about your NGS data. We come from top academic institutions (UCSD, UCLA, Stanford, and MSU)
Based in Berkeley, CA
Our laboratory is conveniently located next to many top biotech companies and world-renowned academic institutions.