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HiPR: High-throughput probabilistic RNA structure inference
被引:0
|作者:
Kuksa, Pavel P.
[1
]
Li, Fan
[4
]
Kannan, Sampath
[2
]
Gregory, Brian D.
[3
]
Leung, Yuk Yee
[1
]
Wang, Li-San
[1
,2
]
机构:
[1] Univ Penn, Penn Neurodegenerat Genom Ctr, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Comp & Informat Sci, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[4] Childrens Hosp Los Angeles, Los Angeles, CA 90027 USA
关键词:
High-throughput structure-sensitive sequencing;
RNA structure inference;
Probabilistic modeling;
DMS-seq;
DMS-MaPseq;
SELECTIVE 2'-HYDROXYL ACYLATION;
SECONDARY STRUCTURE PREDICTION;
PRIMER EXTENSION;
IN-VIVO;
SHAPE-MAP;
CONSTRAINTS;
BINDING;
D O I:
10.1016/j.csbj.2020.06.004
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Recent high-throughput structure-sensitive genome-wide sequencing-based assays have enabled large-scale studies of RNA structure, and robust transcriptome-wide computational prediction of individual RNA structures across RNA classes from these assays has potential to further improve the prediction accuracy. Here, we describe HiPR, a novel method for RNA structure prediction at single-nucleotide resolution that combines high-throughput structure probing data (DMS-seq, DMS-MaPseq) with a novel probabilistic folding algorithm. On validation data spanning a variety of RNA classes, HiPR often increases accuracy for predicting RNA structures, giving researchers new tools to study RNA structure. (C) 2020 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
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页码:1539 / 1547
页数:9
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