Evidence map›Paper›PMID 18979204›Full record

ReviewMolecular biotechnology2009

Informatic resources for identifying and annotating structural RNA motifs.

Ajish D George, Scott A Tenenbaum

Abstract readReview
In one paragraph

Review in Molecular biotechnology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Computational Methods for CLIP-seq Data Processing.Bioinformatics and biology insights · 2014
    Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Ajish D GeorgeGen*NY*Sis Center for Excellence in Cancer Genomics, Department of Biomedical Sciences, School of Public Health, University at Albany-SUNY, 1 Discovery Drive, Room 220, Rensselaer, NY 12144, USA.
Scott A Tenenbaum

Funding

Comprehensive Identification of ENCODE RNA based Cis-Regulatory ElementsU01HG004571 · NHGRI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI TENENBAUM, SCOTT A · 2007 to 2011
$2.6M
NHGRI NIH HHS U01 HG004571NHGRI NIH HHS U01HG004571
6 · The paper itself

Abstract

Post-transcriptional regulation of genes and transcripts is a vital aspect of cellular processes, and unlike transcriptional regulation, remains a largely unexplored domain. One of the most obvious and most important questions to explore is the discovery of functional RNA elements. Many RNA elements have been characterized to date ranging from cis-regulatory motifs within mRNAs to large families of non-coding RNAs. Like protein coding genes, the functional motifs of these RNA elements are highly conserved, but unlike protein coding genes, it is most often the structure and not the sequence that is conserved. Proper characterization of these structural RNA motifs is both the key and the limiting step to understanding the post-transcriptional aspects of the genomic world. Here, we focus on the task of structural motif discovery and provide a survey of the informatics resources geared towards this task.

Indexed as

Databases, Nucleic AcidNucleic Acid ConformationComputational BiologyInternetRNARNA-Binding ProteinsRNARNA-Binding Proteins

Identifiers

PMID18979204
PMCPMC2770092

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.