首页 | 本学科首页   官方微博 | 高级检索  
     


Sequence verification of synthetic DNA by assembly of sequencing reads
Authors:Mandy L. Wilson  Yizhi Cai  Regina Hanlon  Samantha Taylor  Bastien Chevreux  Jo?o C. Setubal  Brett M. Tyler  Jean Peccoud
Affiliation:1.Virginia Bioinformatics Institute, Virginia Tech, Washington Street MC 0477, Blacksburg, VA 24061, USA, 2.DSM Nutritional Products Ltd., Department for Human Nutrition & Health, P.O. Box 2676, CH-4002 Basel, Switzerland, 3.Center for Genome Research and Biocomputing, 3021 Agriculture and Life Sciences Building, Oregon State University, Corvallis, OR 97331-7303 and 4.ICTAS Center for Systems Biology of Engineered Tissues, MC 0193 Virginia Tech, Blacksburg, VA 24061, USA
Abstract: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.
Keywords:
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号