Evidence map›Paper›PMID 21325301›Full record

ArticleBioinformatics (Oxford, England)2011

Annotating genes and genomes with DNA sequences extracted from biomedical articles.

Maximilian Haeussler, Martin Gerner, Casey M Bergman

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Interactive tools for functional annotation of bacterial genomes.Database : the journal of biological databases and curation · 2024
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  12. Translational web robots for pathogen genome analysis.Microbial informatics and experimentation · 2011
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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

3 authors.

Maximilian HaeusslerFaculty of Life Sciences, University of Manchester, Manchester, UK. maximilianh@gmail.com
Martin Gerner
Casey M Bergman

Funding

Biotechnology and Biological Sciences Research Council BB/E012868/1Biotechnology and Biological Sciences Research Council BB/G000093/1
6 · The paper itself

Abstract

motivationIncreasing rates of publication and DNA sequencing make the problem of finding relevant articles for a particular gene or genomic region more challenging than ever. Existing text-mining approaches focus on finding gene names or identifiers in English text. These are often not unique and do not identify the exact genomic location of a study.

resultsHere, we report the results of a novel text-mining approach that extracts DNA sequences from biomedical articles and automatically maps them to genomic databases. We find that ∼20% of open access articles in PubMed central (PMC) have extractable DNA sequences that can be accurately mapped to the correct gene (91%) and genome (96%). We illustrate the utility of data extracted by text2genome from more than 150 000 PMC articles for the interpretation of ChIP-seq data and the design of quantitative reverse transcriptase (RT)-PCR experiments.

conclusionOur approach links articles to genes and organisms without relying on gene names or identifiers. It also produces genome annotation tracks of the biomedical literature, thereby allowing researchers to use the power of modern genome browsers to access and analyze publications in the context of genomic data. AVAILABILITY AND IMPLEMENTATION: Source code is available under a BSD license from http://sourceforge.net/projects/text2genome/ and results can be browsed and downloaded at http://text2genome.org.

Indexed as

GenesGenomeMolecular Sequence AnnotationPubMedBase SequenceChromatin ImmunoprecipitationDatabases, Nucleic AcidData MiningDNAReverse Transcriptase Polymerase Chain ReactionSequence Analysis, DNASoftwareDNA

Identifiers

PMID21325301
PMCPMC3065681

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.