Evidence map›Paper›PMID 25700273›Full record

ArticlePloS one2015

Quality control test for sequence-phenotype assignments.

Maria Teresa Lara Ortiz, Pablo Benjamín Leon Rosario, Pablo Luna-Nevarez, Alba Savin Gamez, Ana Martínez-del Campo, Gabriel Del Rio

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Saturation Mutagenesis of the Transmembrane Region of HokC inInternational journal of molecular sciences · 2021
    Article
  2. Article
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

6 authors.

Maria Teresa Lara OrtizDepartment of Biochemistry and Structural Biology. Instituto de Fisiología Celular at the Universidad Nacional Autónoma de México, México DF, 04510, México.
Pablo Benjamín Leon RosarioDepartment of Biochemistry and Structural Biology. Instituto de Fisiología Celular at the Universidad Nacional Autónoma de México, México DF, 04510, México.
Pablo Luna-NevarezDepartment of agronomical sciences and veterinary. Sonora Institute of Technology, Obregon city 85000, Mexico.
Alba Savin GamezDepartment of Biochemistry and Structural Biology. Instituto de Fisiología Celular at the Universidad Nacional Autónoma de México, México DF, 04510, México.
Ana Martínez-del CampoDepartment of Genetics. Instituto de Fisiología Celular at the Universidad Nacional Autónoma de México, México DF, 04510, México.
Gabriel Del RioDepartment of Biochemistry and Structural Biology. Instituto de Fisiología Celular at the Universidad Nacional Autónoma de México, México DF, 04510, México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relating a gene mutation to a phenotype is a common task in different disciplines such as protein biochemistry. In this endeavour, it is common to find false relationships arising from mutations introduced by cells that may be depurated using a phenotypic assay; yet, such phenotypic assays may introduce additional false relationships arising from experimental errors. Here we introduce the use of high-throughput DNA sequencers and statistical analysis aimed to identify incorrect DNA sequence-phenotype assignments and observed that 10-20% of these false assignments are expected in large screenings aimed to identify critical residues for protein function. We further show that this level of incorrect DNA sequence-phenotype assignments may significantly alter our understanding about the structure-function relationship of proteins. We have made available an implementation of our method at http://bis.ifc.unam.mx/en/software/chispas.

Indexed as

User-Computer InterfaceDNAHigh-Throughput Nucleotide SequencingInternetMutagenesisPhenotypeProteinsQuality ControlSequence Analysis, DNADNAProteins

Identifiers

PMID25700273
PMCPMC4336291

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.