Evidence map›Paper›PMID 24359548›Full record

ArticleMobile DNA2013

A pipeline of programs for collecting and analyzing group II intron retroelement sequences from GenBank.

Michael Abebe, Manuel A Candales, Adrian Duong, Keyar S Hood, Tony Li, Ryan A E Neufeld, Abat Shakenov, Runda Sun, Li Wu, Ashley M Jarding and 2 more

Open access · goldAbstract read
In one paragraph

Article in Mobile DNA, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Michael AbebeDepartment of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Manuel A Candales *Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Adrian Duong *Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Keyar S Hood *Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Tony Li *Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Ryan A E NeufeldDepartment of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Abat Shakenov *Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Runda Sun *Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Li WuDepartment of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Ashley M JardingDepartment of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Cameron SemperDepartment of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
Steven ZimmerlyDepartment of Biological Sciences, University of Calgary, Calgary, AB T2N 1 N4, Canada.
University of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate and complete identification of mobile elements is a challenging task in the current era of sequencing, given their large numbers and frequent truncations. Group II intron retroelements, which consist of a ribozyme and an intron-encoded protein (IEP), are usually identified in bacterial genomes through their IEP; however, the RNA component that defines the intron boundaries is often difficult to identify because of a lack of strong sequence conservation corresponding to the RNA structure. Compounding the problem of boundary definition is the fact that a majority of group II intron copies in bacteria are truncated.

resultsHere we present a pipeline of 11 programs that collect and analyze group II intron sequences from GenBank. The pipeline begins with a BLAST search of GenBank using a set of representative group II IEPs as queries. Subsequent steps download the corresponding genomic sequences and flanks, filter out non-group II introns, assign introns to phylogenetic subclasses, filter out incomplete and/or non-functional introns, and assign IEP sequences and RNA boundaries to the full-length introns. In the final step, the redundancy in the data set is reduced by grouping introns into sets of ≥95% identity, with one example sequence chosen to be the representative.

conclusionsThese programs should be useful for comprehensive identification of group II introns in sequence databases as data continue to rapidly accumulate.

Identifiers

PMID24359548
PMCPMC4028801
OpenAlexW2143861586

What OpenQuestion holds

Textmetadata
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.