Journal Article FZJ-2020-02633

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Evaluating DCA-based method performances for RNA contact prediction by a well-curated data set

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2020
HighWire Press Stanford, Calif.

RNA 26(7), 794 - 802 () [10.1261/rna.073809.119]

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Abstract: RNA molecules play many pivotal roles in a cell that are still not fully understood. Any detailed understanding of RNA function requires knowledge of its three-dimensional structure, yet experimental RNA structure resolution remains demanding. Recent advances in sequencing provide unprecedented amounts of sequence data that can be statistically analyzed by methods such as direct coupling analysis (DCA) to determine spatial proximity or contacts of specific nucleic acid pairs, which improve the quality of structure prediction. To quantify this structure prediction improvement, we here present a well curated data set of about 70 RNA structures of high resolution and compare different nucleotide–nucleotide contact prediction methods available in the literature. We observe only minor differences between the performances of the different methods. Moreover, we discuss how robust these predictions are for different contact definitions and how strongly they depend on procedures used to curate and align the families of homologous RNA sequences.

Classification:

Contributing Institute(s):
  1. Jülich Supercomputing Center (JSC)
Research Program(s):
  1. 511 - Computational Science and Mathematical Methods (POF3-511) (POF3-511)
  2. Forschergruppe Schug (hkf6_20170901) (hkf6_20170901)
  3. PhD no Grant - Doktorand ohne besondere Förderung (PHD-NO-GRANT-20170405) (PHD-NO-GRANT-20170405)

Appears in the scientific report 2020
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Medline ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; Essential Science Indicators ; IF < 5 ; JCR ; NCBI Molecular Biology Database ; PubMed Central ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2020-07-27, last modified 2022-09-30