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Inexpensive Multiplexed Library Preparation for Megabase-Sized Genomes
Author(s) -
Michael Baym,
Sergey Kryazhimskiy,
Tami D. Lieberman,
Hattie Chung,
Michael M. Desai,
Roy Kishony
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0128036
Subject(s) - amplicon , genome , biology , dna sequencing , computational biology , deep sequencing , amplicon sequencing , pyrosequencing , genomic library , genomics , massive parallel sequencing , genetics , polymerase chain reaction , dna , gene , base sequence , 16s ribosomal rna
Whole-genome sequencing has become an indispensible tool of modern biology. However, the cost of sample preparation relative to the cost of sequencing remains high, especially for small genomes where the former is dominant. Here we present a protocol for rapid and inexpensive preparation of hundreds of multiplexed genomic libraries for Illumina sequencing. By carrying out the Nextera tagmentation reaction in small volumes, replacing costly reagents with cheaper equivalents, and omitting unnecessary steps, we achieve a cost of library preparation of $8 per sample, approximately 6 times cheaper than the standard Nextera XT protocol. Furthermore, our procedure takes less than 5 hours for 96 samples. Several hundred samples can then be pooled on the same HiSeq lane via custom barcodes. Our method will be useful for re-sequencing of microbial or viral genomes, including those from evolution experiments, genetic screens, and environmental samples, as well as for other sequencing applications including large amplicon, open chromosome, artificial chromosomes, and RNA sequencing.

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