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Sequence verification of synthetic DNA by assembly of sequencing reads

Gene synthesis attempts to assemble user-defined DNA sequences with base-level precision. Verifying the sequences of construction intermediates and the final product of a gene synthesis project is a critical part of the workflow, yet one that has received the least attention. Sequence validation is...

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Autores principales: Wilson, Mandy L., Cai, Yizhi, Hanlon, Regina, Taylor, Samantha, Chevreux, Bastien, Setubal, João C., Tyler, Brett M., Peccoud, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592409/
https://www.ncbi.nlm.nih.gov/pubmed/23042248
http://dx.doi.org/10.1093/nar/gks908
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author Wilson, Mandy L.
Cai, Yizhi
Hanlon, Regina
Taylor, Samantha
Chevreux, Bastien
Setubal, João C.
Tyler, Brett M.
Peccoud, Jean
author_facet Wilson, Mandy L.
Cai, Yizhi
Hanlon, Regina
Taylor, Samantha
Chevreux, Bastien
Setubal, João C.
Tyler, Brett M.
Peccoud, Jean
author_sort Wilson, Mandy L.
collection PubMed
description Gene synthesis attempts to assemble user-defined DNA sequences with base-level precision. Verifying the sequences of construction intermediates and the final product of a gene synthesis project is a critical part of the workflow, yet one that has received the least attention. Sequence validation is equally important for other kinds of curated clone collections. Ensuring that the physical sequence of a clone matches its published sequence is a common quality control step performed at least once over the course of a research project. GenoREAD is a web-based application that breaks the sequence verification process into two steps: the assembly of sequencing reads and the alignment of the resulting contig with a reference sequence. GenoREAD can determine if a clone matches its reference sequence. Its sophisticated reporting features help identify and troubleshoot problems that arise during the sequence verification process. GenoREAD has been experimentally validated on thousands of gene-sized constructs from an ORFeome project, and on longer sequences including whole plasmids and synthetic chromosomes. Comparing GenoREAD results with those from manual analysis of the sequencing data demonstrates that GenoREAD tends to be conservative in its diagnostic. GenoREAD is available at www.genoread.org.
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spelling pubmed-35924092013-03-08 Sequence verification of synthetic DNA by assembly of sequencing reads Wilson, Mandy L. Cai, Yizhi Hanlon, Regina Taylor, Samantha Chevreux, Bastien Setubal, João C. Tyler, Brett M. Peccoud, Jean Nucleic Acids Res Methods Online Gene synthesis attempts to assemble user-defined DNA sequences with base-level precision. Verifying the sequences of construction intermediates and the final product of a gene synthesis project is a critical part of the workflow, yet one that has received the least attention. Sequence validation is equally important for other kinds of curated clone collections. Ensuring that the physical sequence of a clone matches its published sequence is a common quality control step performed at least once over the course of a research project. GenoREAD is a web-based application that breaks the sequence verification process into two steps: the assembly of sequencing reads and the alignment of the resulting contig with a reference sequence. GenoREAD can determine if a clone matches its reference sequence. Its sophisticated reporting features help identify and troubleshoot problems that arise during the sequence verification process. GenoREAD has been experimentally validated on thousands of gene-sized constructs from an ORFeome project, and on longer sequences including whole plasmids and synthetic chromosomes. Comparing GenoREAD results with those from manual analysis of the sequencing data demonstrates that GenoREAD tends to be conservative in its diagnostic. GenoREAD is available at www.genoread.org. Oxford University Press 2013-01 2012-10-05 /pmc/articles/PMC3592409/ /pubmed/23042248 http://dx.doi.org/10.1093/nar/gks908 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Wilson, Mandy L.
Cai, Yizhi
Hanlon, Regina
Taylor, Samantha
Chevreux, Bastien
Setubal, João C.
Tyler, Brett M.
Peccoud, Jean
Sequence verification of synthetic DNA by assembly of sequencing reads
title Sequence verification of synthetic DNA by assembly of sequencing reads
title_full Sequence verification of synthetic DNA by assembly of sequencing reads
title_fullStr Sequence verification of synthetic DNA by assembly of sequencing reads
title_full_unstemmed Sequence verification of synthetic DNA by assembly of sequencing reads
title_short Sequence verification of synthetic DNA by assembly of sequencing reads
title_sort sequence verification of synthetic dna by assembly of sequencing reads
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592409/
https://www.ncbi.nlm.nih.gov/pubmed/23042248
http://dx.doi.org/10.1093/nar/gks908
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