For DNA sequencing we are proudly distributing LoopGenomics kits and services that enable long read sequencing on Illumina sequencers.
With its proprietary technology, LoopGenomics:
Overview technology
Attach
Every sample is exposed to millions of unique barcodes, but only one barcode attaches per DNA molecule.
Amplify
Every molecule, along with its unique barcode, is amplified using PCR.
Distribute
For each molecule copy, the barcode is randomly distributed within the molecule.
Sequence
Sequence the segment next to each barcode.
Assemble
Short reads that share the same barcode are combined algorithmically into a full-length molecule using linked-read de-novo assembly
The Loop Genomics technology is offered as library preparation kits and as a sequencing service.
When using the kit format, this is the workflow:
When using the service format, this is the workflow:
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