Source: Agilent Technologies
Improve next-generation sequencing results by making smarter decisions about library size and read length before you ever start a run. This guide explains how electrophoretic QC and smear analysis with the Agilent 5200 Fragment Analyzer System can predict and prevent “sequencing through the insert,” a common problem that introduces adapter contamination and degrades data quality. By evaluating library size distributions, you can better estimate how fragments will behave under different run settings and avoid unnecessary noise and wasted sequencing resources.
Read the full application note to learn how smear analysis helps you align library preparation with sequencing parameters for cleaner, more reliable NGS data.
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