Evidence map›Paper›PMID 29383564›Full record

ArticleInterdisciplinary sciences, computational life sciences2018

Large Scale Analyses and Visualization of Adaptive Amino Acid Changes Projects.

Noé Vázquez, Cristina P Vieira, Bárbara S R Amorim, André Torres, Hugo López-Fernández, Florentino Fdez-Riverola, José L R Sousa, Miguel Reboiro-Jato, Jorge Vieira

Abstract read
In one paragraph

Article in Interdisciplinary sciences, computational life sciences, 2018. 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. Article
  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

9 authors.

Noé VázquezESEI - Escuela Superior de Ingeniería Informática, Edificio Politécnico, Universidade de Vigo, Campus Universitario As Lagoas s/n, 32004, Ourense, Spain.
Cristina P VieiraInstituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.
Bárbara S R AmorimInstituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.
André TorresInstituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.
Hugo López-FernándezESEI - Escuela Superior de Ingeniería Informática, Edificio Politécnico, Universidade de Vigo, Campus Universitario As Lagoas s/n, 32004, Ourense, Spain.
Florentino Fdez-RiverolaESEI - Escuela Superior de Ingeniería Informática, Edificio Politécnico, Universidade de Vigo, Campus Universitario As Lagoas s/n, 32004, Ourense, Spain.
José L R SousaInstituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.
Miguel Reboiro-JatoESEI - Escuela Superior de Ingeniería Informática, Edificio Politécnico, Universidade de Vigo, Campus Universitario As Lagoas s/n, 32004, Ourense, Spain.
Jorge VieiraInstituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal. jbvieira@ibmc.up.pt.ORCID http://orcid.org/0000-0001-7032-5220

Funding

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia Post-Doc grantFEDER Norte-01-0145-FEDER-000008 - Porto Neurosciences and Neurologic Disease Research Initiative at I3SSpanish Ministry of Economy and Competitiveness TIN2013-47153-C3-3-R
6 · The paper itself

Abstract

When changes at few amino acid sites are the target of selection, adaptive amino acid changes in protein sequences can be identified using maximum-likelihood methods based on models of codon substitution (such as codeml). Although such methods have been employed numerous times using a variety of different organisms, the time needed to collect the data and prepare the input files means that tens or hundreds of coding regions are usually analyzed. Nevertheless, the recent availability of flexible and easy to use computer applications that collect relevant data (such as BDBM) and infer positively selected amino acid sites (such as ADOPS), means that the entire process is easier and quicker than before. However, the lack of a batch option in ADOPS, here reported, still precludes the analysis of hundreds or thousands of sequence files. Given the interest and possibility of running such large-scale projects, we have also developed a database where ADOPS projects can be stored. Therefore, this study also presents the B+ database, which is both a data repository and a convenient interface that looks at the information contained in ADOPS projects without the need to download and unzip the corresponding ADOPS project file. The ADOPS projects available at B+ can also be downloaded, unzipped, and opened using the ADOPS graphical interface. The availability of such a database ensures results repeatability, promotes data reuse with significant savings on the time needed for preparing datasets, and effortlessly allows further exploration of the data contained in ADOPS projects.

Indexed as

Amino AcidsAnimalsBase SequenceDatabases as TopicDrosophilaUser-Computer InterfaceAmino AcidsADOPSB+ databaseOpen dataPositive selection

Identifiers

PMID29383564
PMCPMC5838210

What Socratic 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 Socratic graph.