Evidence map›Paper›PMID 37729135›Full record

ArticlePloS one2023

AlignStatPlot: An R package and online tool for robust sequence alignment statistics and innovative visualization of big data.

Alsamman M Alsamman, Achraf El Allali, Morad M Mokhtar, Khaled Al-Sham'aa, Ahmed E Nassar, Khaled H Mousa, Zakaria Kehel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. 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
1.2field-weighted citation impact, top 20% of its field
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, 8 citations in OpenAlex.

  1. Article
  2. A novelAutophagy · 2025
    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

7 authors at 2 institutions in 2 countries.

Alsamman M AlsammanAgricultural Genetic Engineering Research Institute, Giza, Egypt.ORCID 0000-0002-7765-5035
Achraf El AllaliAfrican Genome Center, Mohammed VI Polytechnic University, Ben Guerir, Morocco.
Morad M MokhtarAgricultural Genetic Engineering Research Institute, Giza, Egypt.
Khaled Al-Sham'aaInternational Center for Agriculture Research in the Dry Areas, Giza, Egypt.
Ahmed E NassarAgricultural Genetic Engineering Research Institute, Giza, Egypt.
Khaled H MousaAgricultural Genetic Engineering Research Institute, Giza, Egypt.
Zakaria KehelInternational Center for Agriculture Research in the Dry Areas, Giza, Egypt.
Agricultural Genetic Engineering Research Institute · EGUniversité Mohammed VI Polytechnique · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sequence alignment (MSA) is essential for understanding genetic variations controlling phenotypic traits in all living organisms. The post-analysis of MSA results is a difficult step for researchers who do not have programming skills. Especially those working with large scale data and looking for potential variations or variable sample groups. Generating bi-allelic data and the comparison of wild and alternative gene forms are important steps in population genetics. Customising MSA visualisation for a single page view is difficult, making viewing potential indels and variations challenging. There are currently no bioinformatics tools that permit post-MSA analysis, in which data on gene and single nucleotide scales could be combined with gene annotations and used for cluster analysis. We introduce "AlignStatPlot," a new R package and online tool that is well-documented and easy-to use for MSA and post-MSA analysis. This tool performs both traditional and cutting-edge analyses on sequencing data and generates new visualisation methods for MSA results. When compared to currently available tools, AlignStatPlot provides a robust ability to handle and visualise diversity data, while the online version will save time and encourage researchers to focus on explaining their findings. It is a simple tool that can be used in conjunction with population genetics software.

Indexed as

Big DataComputational BiologyAllelesCluster AnalysisSequence Alignment

Identifiers

PMID37729135
PMCPMC10511070
OpenAlexW4386884279

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.