Inexpensive multiplexed library preparation for megabase-sized genomes.

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...

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Main Authors: Michael Baym, Sergey Kryazhimskiy, Tami D Lieberman, Hattie Chung, Michael M Desai, Roy Kishony
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4441430?pdf=render
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spelling doaj-3cf976a4a6964e2da5394c32694fdc7e2020-11-25T01:24:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01105e012803610.1371/journal.pone.0128036Inexpensive multiplexed library preparation for megabase-sized genomes.Michael BaymSergey KryazhimskiyTami D LiebermanHattie ChungMichael M DesaiRoy KishonyWhole-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.http://europepmc.org/articles/PMC4441430?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Michael Baym
Sergey Kryazhimskiy
Tami D Lieberman
Hattie Chung
Michael M Desai
Roy Kishony
spellingShingle Michael Baym
Sergey Kryazhimskiy
Tami D Lieberman
Hattie Chung
Michael M Desai
Roy Kishony
Inexpensive multiplexed library preparation for megabase-sized genomes.
PLoS ONE
author_facet Michael Baym
Sergey Kryazhimskiy
Tami D Lieberman
Hattie Chung
Michael M Desai
Roy Kishony
author_sort Michael Baym
title Inexpensive multiplexed library preparation for megabase-sized genomes.
title_short Inexpensive multiplexed library preparation for megabase-sized genomes.
title_full Inexpensive multiplexed library preparation for megabase-sized genomes.
title_fullStr Inexpensive multiplexed library preparation for megabase-sized genomes.
title_full_unstemmed Inexpensive multiplexed library preparation for megabase-sized genomes.
title_sort inexpensive multiplexed library preparation for megabase-sized genomes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description 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.
url http://europepmc.org/articles/PMC4441430?pdf=render
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