In cooperation with Celemics, we offer a sequencing service using barcodes. This is a unique technology called BTseq™ (Barcode-Tagged Sequencing), which is a specific method for very cheap NGS sequencing of templates up to 50 kbp.
This technology fills the space between Sanger sequencing and NGS. Compared to Sanger sequencing, it generates longer stretches in less time while achieving the same accuracy. The advantage over NGS is the low cost and lack of the need for complex bioinformatics processing. Samples can be e.g. plasmids, PCR products and short genomes of e.g. viruses or bacteria.
In cooperation with Celemics, we offer a sequencing service using barcodes. This is a unique technology called BTseq™ (Barcode-Tagged Sequencing), which is a specific method for very cheap NGS sequencing of templates up to 50 kbp.
This technology fills the space between Sanger sequencing and NGS. Compared to Sanger sequencing, it generates longer stretches in less time while achieving the same accuracy. The advantage over NGS is the low cost and lack of the need for complex bioinformatics processing. Samples can be e.g. plasmids, PCR products and short genomes of e.g. viruses or bacteria.