Cross-Site Evaluation of Commercial Sanger Sequencing Chemistries.

BigDye alternative BrightDye BrilliantDye Sanger chemistry replacement Sanger dye evaluation

Journal

Journal of biomolecular techniques : JBT
ISSN: 1943-4731
Titre abrégé: J Biomol Tech
Pays: United States
ID NLM: 100888641

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 25 8 2020
medline: 7 8 2021
entrez: 25 8 2020
Statut: ppublish

Résumé

Sanger sequencing remains an essential tool utilized by researchers. Despite competition from commercial sequencing providers, many academic sequencing core facilities continue to offer these services based on a model of competitive pricing, knowledgeable technical support, and rapid turnaround time. In-house Sanger sequencing remains a viable core service and, until recently, Applied Biosystems BigDye Terminator chemistry was the only commercially available solution for Sanger DNA sequencing on Applied Biosystems (ABI) instruments; however, several new products employing novel dye chemistries and reaction configurations have entered the market. As a result, there is a need to benchmark the performance of these new chemistries on various DNA templates, including difficult-to-sequence templates, and their amenability to commonly employed cost-saving measures, such as dye dilution and reaction miniaturization. To evaluate these new reagents, a study was designed to compare the quality of Sanger sequencing data produced by ABI BigDye and commercially available kits from 2 other vendors using both control and difficult-to-sequence DNA templates under various reaction conditions. This study will serve as a valuable resource to core facilities conducting Sanger sequencing that wish to evaluate the use of an alternative chemistry in their sequencing core.

Identifiants

pubmed: 32831655
doi: 10.7171/jbt.20-3103-002
pii: JBT_2020-3103-002
pmc: PMC7351326
doi:

Substances chimiques

Coloring Agents 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

88-93

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI060354
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA023108
Pays : United States

Informations de copyright

© Association of Biomolecular Resource Facilities.

Références

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pubmed: 9521922
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pubmed: 9521921
J Biomol Tech. 2009 Apr;20(2):116-27
pubmed: 19503623

Auteurs

Jessica W Podnar (JW)

Genomic Sequencing and Analysis Facility, University of Texas, Austin, Texas, USA.

Lorena Pantano (L)

eGenesis Engineering Life, Cambridge, Massachusetts, USA.

Molly J Zeller (MJ)

DNA Sequencing Facility, University of Wisconsin Biotechnology Center, Madison, Wisconsin, USA.

Fred W Kolling (FW)

Genomics and Molecular Biology Shared Resource, Norris Cotton Cancer Center, Geisel School of Medicine, Lebanon, New Hampshire, USA.

Yanping Zhang (Y)

Gene Expression and Genotyping, Interdisciplinary Center for Biotechnology Research, University of Florida, Gainesville, Florida, USA.

Yuriy O Alekseyev (YO)

Department of Pathology and Laboratory Medicine, Boston University, Boston, Massachusetts, USA.

Jeremy Niece (J)

DNA Sequencing Facility, University of Wisconsin Biotechnology Center, Madison, Wisconsin, USA.

Heather Deiderick (H)

Genomic Sequencing and Analysis Facility, University of Texas, Austin, Texas, USA.

Jun Fan (J)

Department of Biomedical Sciences, Genomic Core Facility, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, USA.

Xiaoling Xuei (X)

Indiana University School of Medicine, Indianapolis, Indiana, USA.

Jan Kieleczawa (J)

Wyzer Biosciences, Cambridge, Massachusetts, USA.

Stuart S Levine (SS)

MIT BioMicro Center, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.

Zachary T Herbert (ZT)

Molecular Biology Core Facilities at Dana-Farber Cancer Institute, Boston, Massachusetts, USA; and.

Marie Adams (M)

Genomics Core Facility, Van Andel Institute, Grand Rapids, Michigan, USA.

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Classifications MeSH