Evidence map›Paper›PMID 29280730›Full record

ArticleeLife2017

Phenotype inference in an

Marco Galardini, Alexandra Koumoutsi, Lucia Herrera-Dominguez, Juan Antonio Cordero Varela, Anja Telzerow, Omar Wagih, Morgane Wartel, Olivier Clermont, Erick Denamur, Athanasios Typas and 1 more

Abstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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  19. Temporal encoding of bacterial identity and traits in growth dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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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

11 authors.

Marco GalardiniEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, United Kingdom.ORCID http://orcid.org/0000-0003-2018-8242
Alexandra KoumoutsiGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.ORCID http://orcid.org/0000-0001-8368-4193
Lucia Herrera-DominguezGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Juan Antonio Cordero VarelaEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, United Kingdom.ORCID http://orcid.org/0000-0002-7373-5433
Anja TelzerowGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Omar WagihEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, United Kingdom.
Morgane WartelGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Olivier ClermontINSERM, IAME, UMR1137, Paris, France.
Erick DenamurINSERM, IAME, UMR1137, Paris, France.
Athanasios TypasGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Pedro BeltraoEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, United Kingdom.ORCID http://orcid.org/0000-0002-2724-7703

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding how genetic variation contributes to phenotypic differences is a fundamental question in biology. Combining high-throughput gene function assays with mechanistic models of the impact of genetic variants is a promising alternative to genome-wide association studies. Here we have assembled a large panel of 696

Indexed as

Genetic VariationBiological Variation, PopulationEscherichia coli K12Genetic Complementation TestGenotypePhenotypecomputational biologyE. coligenotype to phenotypeinfectious diseasemicrobiologyphenotypic diversityreference panelsystems biology

Identifiers

PMID29280730
PMCPMC5745082

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.