MAY 11, 2016 6:00 AM PDT

Expanding the molecular toolbox for Nanopore sequencing

Speaker

Abstract

Library preparation for Nanopore sequencing is a very flexible process. There are many ways in which a sequencing template, or other analyte, can be presented to a nanopore for analysis. PCR may or may not be performed, shearing or size selection is not necessary but can be helpful in specific circumstances. You can sequence both strands in a duplex, or just one ... and what’s more, the platform is not limited to just sequencing DNA, but also RNA, and has been used to sense proteins and a wide variety of small molecules. The versatility of the system gives users access to a wide variety of library preparation options, depending on the needs of their experiments: ultra-long reads (>50 kb), low inputs (<50 ng), rapid and simple preps (10 minutes). In this presentation, I discuss the myriad options that are available and enabled with Nanopore sequencing.


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MAY 11, 2016 6:00 AM PDT

Expanding the molecular toolbox for Nanopore sequencing


Specialty

Antibodies

Immunology

Gene Sequencing

Clinical Diagnostics

Cancer Research

Dna Sequencing

Biomarkers

Gene Expression

Cell Culture

Microbiology

Virology

Drug Discovery

Biotechnology

Personalized Medicine

Health

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