Evidence map›Paper›PMID 34432510›Full record

ArticleMolecular biology of the cell2021

CANVS: an easy-to-use application for the analysis and visualization of mass spectrometry-based protein-protein interaction/association data.

Erick F Velasquez, Yenni A Garcia, Ivan Ramirez, Ankur A Gholkar, Jorge Z Torres

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Human REXO4 is Required for Cell Cycle Progression.bioRxiv : the preprint server for biology · 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

5 authors.

Erick F VelasquezDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.
Yenni A GarciaDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.
Ivan RamirezDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.
Ankur A GholkarDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.
Jorge Z TorresDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095.

Funding

TUMOR CELL SURFACES AND CHROMOSOMEST32CA009056 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Gay M Crooks, David A. Nathanson · 1985 to 2026
$10.5M
Investigating the Cell Division MachineryR35GM139539 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 2021 to 2025
$2.2M
Novel Regulatory Factors of the Spindle Assembly CheckpointR01GM117475 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 2016 to 2020
$1.7M
Howard Hughes Medical InstituteNCI NIH HHS T32 CA009056NIGMS NIH HHS R01 GM117475NIGMS NIH HHS R35 GM139539
6 · The paper itself

Abstract

The elucidation of a protein's interaction/association network is important for defining its biological function. Mass spectrometry-based proteomic approaches have emerged as powerful tools for identifying protein-protein interactions (PPIs) and protein-protein associations (PPAs). However, interactome/association experiments are difficult to interpret, considering the complexity and abundance of data that are generated. Although tools have been developed to identify protein interactions/associations quantitatively, there is still a pressing need for easy-to-use tools that allow users to contextualize their results. To address this, we developed CANVS, a computational pipeline that cleans, analyzes, and visualizes mass spectrometry-based interactome/association data. CANVS is wrapped as an interactive Shiny dashboard with simple requirements, allowing users to interface easily with the pipeline, analyze complex experimental data, and create PPI/A networks. The application integrates systems biology databases such as BioGRID and CORUM to contextualize the results. Furthermore, CANVS features a Gene Ontology tool that allows users to identify relevant GO terms in their results and create visual networks with proteins associated with relevant GO terms. Overall, CANVS is an easy-to-use application that benefits all researchers, especially those who lack an established bioinformatic pipeline and are interested in studying interactome/association data.

Indexed as

Computational BiologyGene OntologyGene Regulatory NetworksHumansImage Processing, Computer-AssistedMass SpectrometryProtein Interaction MappingProteinsProteomicsSoftwareSystems BiologyProteins

Identifiers

PMID34432510
PMCPMC8693966

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.