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.
Resources
Targeted Long Read Transcriptome Sequencing with Element LoopSeq™
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Immune Repertoire Sequencing - Element LoopSeq™ Long-Read Sequencing
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Overview of Element LoopSeq™ Long-Read Sequencing Technology
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NGS Replacement for Sanger Sequencing - Matt Kellinger, PhD
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Uncovering the Meta-Transcriptome with Long-Read Sequencing - Shawn Levy, PhD
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