How Automating Agarose Gel Fragment Selection and Sample Analysis Works

Problem: Molecular biology relies on the ability to precisely target and amplify nucleic acids, and next-generation sequencing (NGS) platforms and cloning reactions benefit from precise size selection and analytical characterization of samples. For decades, researchers have used electrophoresis with agarose gels for both size selection and fragment-length distribution assessment of DNA samples for downstream assays.

Written byHamilton Robotics
| 3 min read
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However, in the new era of big science and high-throughput sample processing, the manual work required for electrophoresis is becoming harder to sustain. The associated errors have forced labs with high-throughput pipelines to use new approaches.

Today’s modest labs are conducting at least 3,000 sequencing reactions per year for translational medicine studies, and rerun rates spurred by manual errors can cost millions of dollars.

As a result, upfront sample quality control tests that rely on rapid characterization are crucial for many applications, including miRNA-seq, RNA-seq, ChIP-seq, long-fragment sequencing, gene synthesis and cloning. Reliable size selection for these samples is also critical in maximizing the value of downstream processes.

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