Evidence map›Paper›PMID 28521726›Full record

ArticleBMC genomics2017

OrthoFiller: utilising data from multiple species to improve the completeness of genome annotations.

Michael P Dunne, Steven Kelly

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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  6. Draft Genome Sequence of the Termite-Associated "Cuckoo Fungus,"Microbiology resource announcements · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Michael P DunneDepartment of Plant Sciences, University of Oxford, South Parks Road, Oxford, OX1 3RB, UK.
Steven KellyDepartment of Plant Sciences, University of Oxford, South Parks Road, Oxford, OX1 3RB, UK. steven.kelly@plants.ox.ac.uk.ORCID 0000-0001-8583-5362
University of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backroundComplete and accurate annotation of sequenced genomes is of paramount importance to their utility and analysis. Differences in gene prediction pipelines mean that genome annotations for a species can differ considerably in the quality and quantity of their predicted genes. Furthermore, genes that are present in genome sequences sometimes fail to be detected by computational gene prediction methods. Erroneously unannotated genes can lead to oversights and inaccurate assertions in biological investigations, especially for smaller-scale genome projects, which rely heavily on computational prediction.

resultsHere we present OrthoFiller, a tool designed to address the problem of finding and adding such missing genes to genome annotations. OrthoFiller leverages information from multiple related species to identify those genes whose existence can be verified through comparison with known gene families, but which have not been predicted. By simulating missing gene annotations in real sequence datasets from both plants and fungi we demonstrate the accuracy and utility of OrthoFiller for finding missing genes and improving genome annotations. Furthermore, we show that applying OrthoFiller to existing "complete" genome annotations can identify and correct substantial numbers of erroneously missing genes in these two sets of species.

conclusionsWe show that significant improvements in the completeness of genome annotations can be made by leveraging information from multiple species.

Indexed as

Databases, GeneticArabidopsisGenomicsMolecular Sequence AnnotationSaccharomyces cerevisiaeGene predictionGenome annotationOrthogroupOrthology

Identifiers

PMID28521726
PMCPMC5437544
OpenAlexW2953334583

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.