3.9 Article

Quality scores for 32,000 genomes

期刊

STANDARDS IN GENOMIC SCIENCES
卷 9, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/1944-3277-9-20

关键词

DNA; Sequencing; Database; Quality; Evaluation; Status

资金

  1. Genomic Science Program, U.S. Department of Energy (DOE), Office of Science, Biological and Environmental Research (BER) as part of the Plant Microbe Interfaces Scientific Focus Area
  2. BER's BioEnergy Science Center (BESC) at the Oak Ridge National Laboratory [DE-PS02-06ER64304]
  3. Laboratory Directed Research and Development (LDRD) from Oak Ridge National Laboratory
  4. U.S. Department of Energy [DE-AC05-00OR22725]

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Background: More than 80% of the microbial genomes in GenBank are of 'draft' quality (12,553 draft vs. 2,679 finished, as of October, 2013). We have examined all the microbial DNA sequences available for complete, draft, and Sequence Read Archive genomes in GenBank as well as three other major public databases, and assigned quality scores for more than 30,000 prokaryotic genome sequences. Results: Scores were assigned using four categories: the completeness of the assembly, the presence of full-length rRNA genes, tRNA composition and the presence of a set of 102 conserved genes in prokaryotes. Most (similar to 88%) of the genomes had quality scores of 0.8 or better and can be safely used for standard comparative genomics analysis. We compared genomes across factors that may influence the score. We found that although sequencing depth coverage of over 100x did not ensure a better score, sequencing read length was a better indicator of sequencing quality. With few exceptions, most of the 30,000 genomes have nearly all the 102 essential genes. Conclusions: The score can be used to set thresholds for screening data when analyzing all published genomes and reference data is either not available or not applicable. The scores highlighted organisms for which commonly used tools do not perform well. This information can be used to improve tools and to serve a broad group of users as more diverse organisms are sequenced. Unexpectedly, the comparison of predicted tRNAs across 15,000 high quality genomes showed that anticodons beginning with an 'A' (codons ending with a 'U') are almost non-existent, with the exception of one arginine codon (CGU); this has been noted previously in the literature for a few genomes, but not with the depth found here.

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