Literature DB >> 20547637

DARNED: a DAtabase of RNa EDiting in humans.

Anmol Kiran1, Pavel V Baranov.   

Abstract

MOTIVATION: RNA editing is a phenomenon, which is responsible for the alteration of particular nucleotides in RNA sequences relative to their genomic templates. Recently, a large number of RNA editing instances in humans have been identified using bioinformatic screens and high-throughput experimental investigations utilizing next-generation sequencing technologies. However, the available data on RNA editing are not uniform and difficult to access.
RESULTS: Here, we describe a new database DARNED (DAtabase of RNa EDiting) that provides centralized access to available published data related to RNA editing. RNA editing locations are mapped on the reference human genome. The current release of the database contains information on approximately 42 000 human genome coordinates corresponding to RNA locations that undergo RNA editing, mostly involving adenosine-to-inosine (A-to-I) substitutions. The data can be queried using a range of genomic coordinates, their corresponding functional localization in RNA molecules [Exons, Introns, CoDing Sequence (CDS) and UnTranslated Regions (UTRs)] and information regarding tissue/organ/cell sources where RNA editing has been observed. It is also possible to obtain RNA editing information for a specific gene or an RNA molecule using corresponding accession numbers. Search results provide information on the number of expressed sequence tags (ESTs) supporting edited and genomic bases, functional localization of RNA editing and existence of known single nucleotide polymorphisms (SNPs). Editing data can be explored in UCSC and Ensembl genome browsers, in conjunction with additional data provided by these popular genome browsers. DARNED has been designed for researchers seeking information on RNA editing and for the developers of novel algorithms for its prediction. AVAILABILITY: DARNED is accessible at http://darned.ucc.ie

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Year:  2010        PMID: 20547637     DOI: 10.1093/bioinformatics/btq285

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  131 in total

1.  Accurate identification of A-to-I RNA editing in human by transcriptome sequencing.

Authors:  Jae Hoon Bahn; Jae-Hyung Lee; Gang Li; Christopher Greer; Guangdun Peng; Xinshu Xiao
Journal:  Genome Res       Date:  2011-09-29       Impact factor: 9.043

2.  Base-pairing probability in the microRNA stem region affects the binding and editing specificity of human A-to-I editing enzymes ADAR1-p110 and ADAR2.

Authors:  Soh Ishiguro; Josephine Galipon; Rintaro Ishii; Yutaka Suzuki; Shinji Kondo; Mariko Okada-Hatakeyama; Masaru Tomita; Kumiko Ui-Tei
Journal:  RNA Biol       Date:  2018-07-24       Impact factor: 4.652

3.  Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals.

Authors:  Young Seok Ju; Jong-Il Kim; Sheehyun Kim; Dongwan Hong; Hansoo Park; Jong-Yeon Shin; Seungbok Lee; Won-Chul Lee; Sujung Kim; Saet-Byeol Yu; Sung-Soo Park; Seung-Hyun Seo; Ji-Young Yun; Hyun-Jin Kim; Dong-Sung Lee; Maryam Yavartanoo; Hyunseok Peter Kang; Omer Gokcumen; Diddahally R Govindaraju; Jung Hee Jung; Hyonyong Chong; Kap-Seok Yang; Hyungtae Kim; Charles Lee; Jeong-Sun Seo
Journal:  Nat Genet       Date:  2011-07-03       Impact factor: 38.330

4.  RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues.

Authors:  Keren Yizhak; François Aguet; Jaegil Kim; Julian M Hess; Kirsten Kübler; Jonna Grimsby; Ruslana Frazer; Hailei Zhang; Nicholas J Haradhvala; Daniel Rosebrock; Dimitri Livitz; Xiao Li; Eila Arich-Landkof; Noam Shoresh; Chip Stewart; Ayellet V Segrè; Philip A Branton; Paz Polak; Kristin G Ardlie; Gad Getz
Journal:  Science       Date:  2019-06-07       Impact factor: 47.728

5.  circMeta: a unified computational framework for genomic feature annotation and differential expression analysis of circular RNAs.

Authors:  Li Chen; Feng Wang; Emily C Bruggeman; Chao Li; Bing Yao
Journal:  Bioinformatics       Date:  2020-01-15       Impact factor: 6.937

Review 6.  Single-nucleotide variants in human RNA: RNA editing and beyond.

Authors:  Yan Guo; Hui Yu; David C Samuels; Wei Yue; Scott Ness; Ying-Yong Zhao
Journal:  Brief Funct Genomics       Date:  2019-02-14       Impact factor: 4.241

7.  Comment on "Widespread RNA and DNA sequence differences in the human transcriptome".

Authors:  Joseph K Pickrell; Yoav Gilad; Jonathan K Pritchard
Journal:  Science       Date:  2012-03-16       Impact factor: 47.728

8.  Transcriptome-wide identification of A > I RNA editing sites by inosine specific cleavage.

Authors:  Pierre B Cattenoz; Ryan J Taft; Eric Westhof; John S Mattick
Journal:  RNA       Date:  2012-12-21       Impact factor: 4.942

9.  miR-EdiTar: a database of predicted A-to-I edited miRNA target sites.

Authors:  Alessandro Laganà; Alessio Paone; Dario Veneziano; Luciano Cascione; Pierluigi Gasparini; Stefania Carasi; Francesco Russo; Giovanni Nigita; Valentina Macca; Rosalba Giugno; Alfredo Pulvirenti; Dennis Shasha; Alfredo Ferro; Carlo M Croce
Journal:  Bioinformatics       Date:  2012-10-07       Impact factor: 6.937

10.  EndoVIPER-seq for Improved Detection of A-to-I Editing Sites in Cellular RNA.

Authors:  Steve D Knutson; Jennifer M Heemstra
Journal:  Curr Protoc Chem Biol       Date:  2020-06
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