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Experimental Design-Based Functional Mining and Characterization of High-Throughput Sequencing Data in the Sequence Read Archive

Overview of attention for article published in PLOS ONE, October 2013
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Title
Experimental Design-Based Functional Mining and Characterization of High-Throughput Sequencing Data in the Sequence Read Archive
Published in
PLOS ONE, October 2013
DOI 10.1371/journal.pone.0077910
Pubmed ID
Authors

Takeru Nakazato, Tazro Ohta, Hidemasa Bono

Abstract

High-throughput sequencing technology, also called next-generation sequencing (NGS), has the potential to revolutionize the whole process of genome sequencing, transcriptomics, and epigenetics. Sequencing data is captured in a public primary data archive, the Sequence Read Archive (SRA). As of January 2013, data from more than 14,000 projects have been submitted to SRA, which is double that of the previous year. Researchers can download raw sequence data from SRA website to perform further analyses and to compare with their own data. However, it is extremely difficult to search entries and download raw sequences of interests with SRA because the data structure is complicated, and experimental conditions along with raw sequences are partly described in natural language. Additionally, some sequences are of inconsistent quality because anyone can submit sequencing data to SRA with no quality check. Therefore, as a criterion of data quality, we focused on SRA entries that were cited in journal articles. We extracted SRA IDs and PubMed IDs (PMIDs) from SRA and full-text versions of journal articles and retrieved 2748 SRA ID-PMID pairs. We constructed a publication list referring to SRA entries. Since, one of the main themes of -omics analyses is clarification of disease mechanisms, we also characterized SRA entries by disease keywords, according to the Medical Subject Headings (MeSH) extracted from articles assigned to each SRA entry. We obtained 989 SRA ID-MeSH disease term pairs, and constructed a disease list referring to SRA data. We previously developed feature profiles of diseases in a system called "Gendoo". We generated hyperlinks between diseases extracted from SRA and the feature profiles of it. The developed project, publication and disease lists resulting from this study are available at our web service, called "DBCLS SRA" (http://sra.dbcls.jp/). This service will improve accessibility to high-quality data from SRA.

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Geographical breakdown

Country Count As %
Germany 2 1%
United States 2 1%
United Kingdom 1 <1%
Netherlands 1 <1%
Japan 1 <1%
Sri Lanka 1 <1%
Unknown 154 95%

Demographic breakdown

Readers by professional status Count As %
Student > Master 30 19%
Student > Ph. D. Student 26 16%
Researcher 22 14%
Student > Bachelor 18 11%
Student > Doctoral Student 8 5%
Other 16 10%
Unknown 42 26%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 39 24%
Agricultural and Biological Sciences 32 20%
Medicine and Dentistry 16 10%
Computer Science 6 4%
Immunology and Microbiology 6 4%
Other 17 10%
Unknown 46 28%