Evidence map›Paper›PMID 21092114›Full record

ArticleBMC genomics2010

POLYAR, a new computer program for prediction of poly(A) sites in human sequences.

Malik Nadeem Akhtar, Syed Abbas Bukhari, Zeeshan Fazal, Raheel Qamar, Ilham A Shahmuradov

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 54 citations in OpenAlex.

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  12. Inference of the human polyadenylation code.Bioinformatics (Oxford, England) · 2018
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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Malik Nadeem AkhtarDepartment of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan.
Syed Abbas Bukhari
Zeeshan Fazal
Raheel Qamar
Ilham A Shahmuradov
COMSATS University Islamabad · PKInstitute of Botany · AZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundmRNA polyadenylation is an essential step of pre-mRNA processing in eukaryotes. Accurate prediction of the pre-mRNA 3'-end cleavage/polyadenylation sites is important for defining the gene boundaries and understanding gene expression mechanisms.

results28761 human mapped poly(A) sites have been classified into three classes containing different known forms of polyadenylation signal (PAS) or none of them (PAS-strong, PAS-weak and PAS-less, respectively) and a new computer program POLYAR for the prediction of poly(A) sites of each class was developed. In comparison with polya_svm (till date the most accurate computer program for prediction of poly(A) sites) while searching for PAS-strong poly(A) sites in human sequences, POLYAR had a significantly higher prediction sensitivity (80.8% versus 65.7%) and specificity (66.4% versus 51.7%) However, when a similar sort of search was conducted for PAS-weak and PAS-less poly(A) sites, both programs had a very low prediction accuracy, which indicates that our knowledge about factors involved in the determination of the poly(A) sites is not sufficient to identify such polyadenylation regions.

conclusionsWe present a new classification of polyadenylation sites into three classes and a novel computer program POLYAR for prediction of poly(A) sites/regions of each of the class. In tests, POLYAR shows high accuracy of prediction of the PAS-strong poly(A) sites, though this program's efficiency in searching for PAS-weak and PAS-less poly(A) sites is not very high but is comparable to other available programs. These findings suggest that additional characteristics of such poly(A) sites remain to be elucidated. POLYAR program with a stand-alone version for downloading is available at http://cub.comsats.edu.pk/polyapredict.htm.

Indexed as

Software5' Untranslated RegionsBase SequenceComputational BiologyHumansIntronsPoly APolyadenylation5' Untranslated RegionsPoly A

Identifiers

PMID21092114
PMCPMC3053588
OpenAlexW1997699426

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.