4.8 Article

A large genome center's improvements to the Illumina sequencing system

Journal

NATURE METHODS
Volume 5, Issue 12, Pages 1005-1010

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nmeth.1270

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Funding

  1. MRC [G0701805] Funding Source: UKRI
  2. Medical Research Council [G0701805] Funding Source: Medline
  3. Wellcome Trust [079643] Funding Source: Medline
  4. Medical Research Council [G0701805] Funding Source: researchfish

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The Wellcome Trust Sanger Institute is one of the world's largest genome centers, and a substantial amount of our sequencing is performed with 'next-generation' massively parallel sequencing technologies: in June 2008 the quantity of purity-filtered sequence data generated by our Genome Analyzer (Illumina) platforms reached 1 terabase, and our average weekly Illumina production output is currently 64 gigabases. Here we describe a set of improvements we have made to the standard Illumina protocols to make the library preparation more reliable in a high-throughput environment, to reduce bias, tighten insert size distribution and reliably obtain high yields of data.

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