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Advancing Human Genomics With Nanopore Sequencing

Advance Human Genomics

High-throughput sequencing has revolutionized the field of human genomics. Yet, technologies must continually aim to close genomic gaps in order to drive new discoveries. 

Traditional short-read sequencing platforms can present challenges, such as read-length limitations which preclude subsequent analysis. However, ultra-long read sequencing delivered by real-time, high-throughput nanopore technology, can facilitate the rapid, accurate characterization of full-length transcripts in a single robust workflow.

This whitepaper highlights specific case studies that reveal how researchers are applying nanopore technology to a variety of sequencing techniques, including whole-genome, targeted, RNA sequencing and single-cell analysis.

Download this whitepaper to discover: 

  • Long-read sequencing approaches for the phasing of large genomic regions 
  • Accurate methods for variant calling and structural analysis
  • Human research applications of nanopore sequencing technology

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