Hear the talk by Loop Genomic’s Indira Wu at ESHG on Monday, June 17, 15:00 – 16:30 in Room A-4.

  • Synthetic long-read NGS kit
  • Uses your existing Illumina sequencer – no extra instruments
  • Multiplex single-tube workflow
  • Consensus error correction – error rates reduced 40x vs short reads
  • Full isoform mapping for transcriptome research
  • True quantitative results due to transcript counting using UMIs and full-
    length reads
  • Better resolution on species and strain level for microbiome research

Loop Genomics has developed a synthetic long-read sequencing technology
that leverages existing Illumina® short read sequencers coupled with LoopSeq®
barcoding technology to enable single-molecule, long-read sequencing on any
Illumina® infrastructure.

Indira Wu, the Director of Molecular Biology at Loop Genomics, will in her talk
explore LoopSeq® sequencing technology and how it provides previously
inaccessible layers of information from Illumina®-generates sequences,
enabling a wide variety of diverse sequencing application, including sequencing
of microbiomes, transcriptomes, targeted amplicons, and more.