RNA structure framework: automated transcriptome-wide reconstruction of RNA secondary structures from high-throughput structure probing data

被引:13
作者
Incarnato, Danny [1 ,2 ]
Neri, Francesco [1 ]
Anselmi, Francesca [1 ,2 ]
Oliviero, Salvatore [1 ,2 ]
机构
[1] Human Genet Fdn HuGeF, I-10126 Turin, Italy
[2] Univ Turin, Dipartimento Sci Vita & Biol Sistemi, I-10123 Turin, Italy
关键词
LONG NONCODING RNAS; STRUCTURE PREDICTION; HUMAN GENOME; LANDSCAPE; FEATURES; REVEALS;
D O I
10.1093/bioinformatics/btv571
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The rapidly increasing number of discovered non-coding RNAs makes the understanding of their structure a key feature toward a deeper comprehension of gene expression regulation. Various enzymatic-and chemically-based approaches have been recently developed to allow whole-genome studies of RNA secondary structures. Several methods have been recently presented that allow high-throughput RNA structure probing (CIRS-seq, Structure-seq, SHAPE-seq, PARS, etc.) and unbiased structural inference of residues within RNAs in their native conformation. We here present an analysis toolkit, named RNA Structure Framework (RSF), which allows fast and fully-automated analysis of high-throughput structure probing data, from data pre-processing to whole-transcriptome RNA structure inference.
引用
收藏
页码:459 / 461
页数:3
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