Please use this identifier to cite or link to this item: 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
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