Long-Read Sequencing

Long-read sequencing provides the additional genomic context that is often needed to reveal the full complexity of biological systems. With LoopSeq, researchers can obtain highly accurate long-read information on a short-read platform without the need for a dedicated instrument.

LoopSeq provides access to:

• Isoform-resolved RNA sequencing data that can detect changes in gene expression that are invisible to short reads.
• Full-length 16S data needed to identify bacteria at the species or strain level.
• Immune repertoire data that reveal the full complexity of the immune response, including isotype or paired heavy and light chains.
• Long-read targeted sequencing data to detect gene fusions and fully phased mutations.