Evidence map›Paper›PMID 31281302›Full record

ArticleFrontiers in microbiology2019

On the Impact of the Pangenome and Annotation Discrepancies While Building Protein Sequence Databases for Bacteria Proteogenomics.

Karla C T Machado, Suereta Fortuin, Gisele Guicardi Tomazella, Andre F Fonseca, Robin Mark Warren, Harald G Wiker, Sandro Jose de Souza, Gustavo Antonio de Souza

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Building pan-genome infrastructures for crop plants and their use in association genetics.DNA research : an international journal for rapid publication of reports on genes and genomes · 2021
    Review
  4. 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

8 authors.

Karla C T MachadoBioinformatics Multidisciplinary Environment, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
Suereta FortuinDST/NRF Centre of Excellence for Biomedical Tuberculosis Research/SAMRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa.
Gisele Guicardi TomazellaBioinformatics Multidisciplinary Environment, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
Andre F FonsecaBioinformatics Multidisciplinary Environment, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
Robin Mark WarrenDST/NRF Centre of Excellence for Biomedical Tuberculosis Research/SAMRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa.
Harald G WikerThe Gade Research Group for Infection and Immunity, Department of Clinical Science, University of Bergen, Bergen, Norway.
Sandro Jose de SouzaBioinformatics Multidisciplinary Environment, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
Gustavo Antonio de SouzaBioinformatics Multidisciplinary Environment, Universidade Federal do Rio Grande do Norte, Natal, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In proteomics, peptide information within mass spectrometry (MS) data from a specific organism sample is routinely matched against a protein sequence database that best represent such organism. However, if the species/strain in the sample is unknown or genetically poorly characterized, it becomes challenging to determine a database which can represent such sample. Building customized protein sequence databases merging multiple strains for a given species has become a strategy to overcome such restrictions. However, as more genetic information is publicly available and interesting genetic features such as the existence of pan- and core genes within a species are revealed, we questioned how efficient such merging strategies are to report relevant information. To test this assumption, we constructed databases containing conserved and unique sequences for 10 different species. Features that are relevant for probabilistic-based protein identification by proteomics were then monitored. As expected, increase in database complexity correlates with pangenomic complexity. However,

Indexed as

databasesmass spectrometrypangenomeproteogenomicsproteomics

Identifiers

PMID31281302
PMCPMC6596428

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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.