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SAG-QC: quality control of single amplified genome information by subtracting non-target sequences based on sequence compositions

Overview of attention for article published in BMC Bioinformatics, March 2017
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Title
SAG-QC: quality control of single amplified genome information by subtracting non-target sequences based on sequence compositions
Published in
BMC Bioinformatics, March 2017
DOI 10.1186/s12859-017-1572-5
Pubmed ID
Authors

Toru Maruyama, Tetsushi Mori, Keisuke Yamagishi, Haruko Takeyama

Abstract

Whole genome amplification techniques have enabled the analysis of unexplored genomic information by sequencing of single-amplified genomes (SAGs). Whole genome amplification of single bacteria is currently challenging because contamination often occurs in experimental processes. Thus, to increase the confidence in the analyses of sequenced SAGs, bioinformatics approaches that identify and exclude non-target sequences from SAGs are required. Since currently reported approaches utilize sequence information in public databases, they have limitations when new strains are the targets of interest. Here, we developed a software SAG-QC that identify and exclude non-target sequences independent of database. In our method, "no template control" sequences acquired during WGA were used. We calculated the probability that a sequence was derived from contaminants by comparing k-mer compositions with the no template control sequences. Based on the results of tests using simulated SAG datasets, the accuracy of our method for predicting non-target sequences was higher than that of currently reported techniques. Subsequently, we applied our tool to actual SAG datasets and evaluated the accuracy of the predictions. Our method works independently of public sequence information for distinguishing SAGs from non-target sequences. This method will be effective when employed against SAG sequences of unexplored strains and we anticipate that it will contribute to the correct interpretation of SAGs.

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Mendeley readers

The data shown below were compiled from readership statistics for 24 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 24 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 17%
Student > Master 4 17%
Student > Bachelor 3 13%
Student > Ph. D. Student 3 13%
Student > Doctoral Student 2 8%
Other 2 8%
Unknown 6 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 17%
Agricultural and Biological Sciences 4 17%
Immunology and Microbiology 3 13%
Medicine and Dentistry 2 8%
Computer Science 1 4%
Other 3 13%
Unknown 7 29%