Evidence map›Paper›PMID 33156866›Full record

ArticlePloS one2020

dagLogo: An R/Bioconductor package for identifying and visualizing differential amino acid group usage in proteomics data.

Jianhong Ou, Haibo Liu, Niraj K Nirala, Alexey Stukalov, Usha Acharya, Michael R Green, Lihua Julie Zhu

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. The regulatory landscape of the yeast phosphoproteome.Nature structural & molecular biology · 2023
    Article
  4. The fitness cost of spurious phosphorylation.bioRxiv : the preprint server for biology · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. 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.

Jianhong OuDepartment of Molecular, Cell, and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.ORCID 0000-0002-8652-2488
Haibo LiuDepartment of Molecular, Cell, and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.ORCID 0000-0002-4213-2883
Niraj K NiralaProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.
Alexey StukalovInstitute of Virology, Technical University of Munich, Munich, Germany.ORCID 0000-0002-4981-8124
Usha AcharyaDepartment of Molecular, Cell, and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.ORCID 0000-0002-4433-4892
Michael R GreenDepartment of Molecular, Cell, and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.
Lihua Julie ZhuDepartment of Molecular, Cell, and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.ORCID 0000-0001-7416-0590

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequence logos have been widely used as graphical representations of conserved nucleic acid and protein motifs. Due to the complexity of the amino acid (AA) alphabet, rich post-translational modification, and diverse subcellular localization of proteins, few versatile tools are available for effective identification and visualization of protein motifs. In addition, various reduced AA alphabets based on physicochemical, structural, or functional properties have been valuable in the study of protein alignment, folding, structure prediction, and evolution. However, there is lack of tools for applying reduced AA alphabets to the identification and visualization of statistically significant motifs. To fill this gap, we developed an R/Bioconductor package dagLogo, which has several advantages over existing tools. First, dagLogo allows various formats for input sets and provides comprehensive options to build optimal background models. It implements different reduced AA alphabets to group AAs of similar properties. Furthermore, dagLogo provides statistical and visual solutions for differential AA (or AA group) usage analysis of both large and small data sets. Case studies showed that dagLogo can better identify and visualize conserved protein sequence patterns from different types of inputs and can potentially reveal the biological patterns that could be missed by other logo generators.

Indexed as

AlgorithmsAmino Acid MotifsAmino AcidsConserved SequenceDatabases, ProteinHumansPosition-Specific Scoring MatricesProteinsProteomicsSequence AlignmentSoftwareAmino AcidsProteins

Identifiers

PMID33156866
PMCPMC7647101

What OpenQuestion holds

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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.