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https://doi.org/10.1186/1471-2164-11-242
Title: | Finishing genomes with limited resources: Lessons from an ensemble of microbial genomes | Authors: | Nagarajan, N Cook, C Di Bonaventura, M Ge, H Richards, A Bishop-Lilly, K.A DeSalle, R Read, T.D Pop, M |
Keywords: | bacterial DNA contig Aggregatibacter aphrophilus article chromatin assembly and disassembly contig mapping DNA sequence Frankia genome mathematical analysis microbial genome nonhuman nucleotide sequence Pantoea pyrosequencing Rickettsia prowazekii Salmonella enterica sequence analysis Vibrio cholerae Yersinia Yersinia aldovae Yersinia bercovieri Yersinia fredriksenii yersinia intermedia yersinia kristensenii Yersinia mollaretii Yersinia pestis Yersinia rohdei Yersinia ruckeri bacterial genome DNA sequence economics Gammaproteobacteria genetics human methodology Rickettsia prowazekii Yersinia Gammaproteobacteria Genome, Bacterial Humans Rickettsia prowazekii Sequence Analysis, DNA Yersinia |
Issue Date: | 2010 | Citation: | Nagarajan, N, Cook, C, Di Bonaventura, M, Ge, H, Richards, A, Bishop-Lilly, K.A, DeSalle, R, Read, T.D, Pop, M (2010). Finishing genomes with limited resources: Lessons from an ensemble of microbial genomes. BMC Genomics 11 (1) : 242. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2164-11-242 | Rights: | Attribution 4.0 International | Abstract: | While new sequencing technologies have ushered in an era where microbial genomes can be easily sequenced, the goal of routinely producing high-quality draft and finished genomes in a cost-effective fashion has still remained elusive. Due to shorter read lengths and limitations in library construction protocols, shotgun sequencing and assembly based on these technologies often results in fragmented assemblies. Correspondingly, while draft assemblies can be obtained in days, finishing can take many months and hence the time and effort can only be justified for high-priority genomes and in large sequencing centers. In this work, we revisit this issue in light of our own experience in producing finished and nearly-finished genomes for a range of microbial species in a small-lab setting. These genomes were finished with surprisingly little investments in terms of time, computational effort and lab work, suggesting that the increased access to sequencing might also eventually lead to a greater proportion of finished genomes from small labs and genomics cores.© 2010 The Article is a work of the United States Government; licensee BioMed Central Ltd. | Source Title: | BMC Genomics | URI: | https://scholarbank.nus.edu.sg/handle/10635/181671 | ISSN: | 14712164 | DOI: | 10.1186/1471-2164-11-242 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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