Evidence map›Paper›PMID 36699377›Full record

ArticleBioinformatics advances2022

Evidente-a visual analytics tool for data enrichment in SNP-based phylogenetic trees.

Mathias Witte Paz, Theresa A Harbig, Kay Nieselt

Open access · goldAbstract read
In one paragraph

Article in Bioinformatics advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

3 authors at 1 institution in 1 country.

Mathias Witte PazInstitute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen 72076, Germany.ORCID https://orcid.org/0000-0001-8113-4139
Theresa A HarbigInstitute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen 72076, Germany.ORCID https://orcid.org/0000-0001-8716-5788
Kay NieseltInstitute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen 72076, Germany.
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: A common practice in the analysis of pathogens and their strains is using single-nucleotide polymorphisms (SNPs) to reconstruct their evolutionary history. However, genome-wide SNP-based phylogenetic trees are rarely analyzed without any further information. Including the underlying SNP data together with further metadata on the respective samples in the exploration process can facilitate linking the genomic and phenotypic properties of the samples. Results: We introduce Efficient VIsual analytics tool for Data ENrichment in phylogenetic TreEs (Evidente), a web-application that provides an interactive visual analysis interface for the simultaneous interrogation of phylogenetic relationships, genome-wide SNP data and metadata for samples of an organism. Besides visualizing the phylogenetic tree, Evidente classifies SNPs as supporting or non-supporting of the tree structures and shows the distribution of both types of SNPs among samples and clades of interest. Furthermore, additional metadata can be included in the visualization. Lastly, Evidente includes an enrichment analysis to identify over-represented genomic features encoded by GO-terms within the clades of the tree. We demonstrate the usability of Evidente with the data of the pathogens Availability and implementation: Evidente is available at the TueVis visualization web server at https://evidente-tuevis.cs.uni-tuebingen.de/, it can also be run locally. Supplementary information: Supplementary data are available at

Identifiers

PMID36699377
PMCPMC9710622
OpenAlexW4306166225

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.