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Chunk #71 — Materials and methods — Illumina HiSeq and MiSeq sequencing — Illumina library construction

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Characterizing and measuring bias in sequence data.
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yes

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For all Illumina PCR-based libraries prepared, the desired insert size was selected by gel electrophoresis with a target of ±10 to 15%. Multiple gel cuts were taken for libraries requiring high sequencing coverage. For the Broad PCR-free method, a second 0.7× SPRI reaction following adapter ligation was utilized instead of gel electrophoresis to tighten up size distribution and reduce excess adapter.