Evidence map›Paper›PMID 33092528›Full record

ArticleBMC bioinformatics2020

PyGNA: a unified framework for geneset network analysis.

Viola Fanfani, Fabio Cassano, Giovanni Stracquadanio

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 90% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 1 country.

Viola FanfaniSchool of Biological Science, The University of Edinburgh, Edinburgh, EH9 3BF, UK.
Fabio CassanoSchool of Biological Science, The University of Edinburgh, Edinburgh, EH9 3BF, UK.
Giovanni StracquadanioSchool of Biological Science, The University of Edinburgh, Edinburgh, EH9 3BF, UK. giovanni.stracquadanio@ed.ac.uk.ORCID http://orcid.org/0000-0001-9819-3645
University of Edinburgh · GB

Funding

Wellcome Trust 207769/A/17/Z
6 · The paper itself

Abstract

backgroundGene and protein interaction experiments provide unique opportunities to study the molecular wiring of a cell. Integrating high-throughput functional genomics data with this information can help identifying networks associated with complex diseases and phenotypes.

resultsHere we introduce an integrated statistical framework to test network properties of single and multiple genesets under different interaction models. We implemented this framework as an open-source software, called Python Geneset Network Analysis (PyGNA). Our software is designed for easy integration into existing analysis pipelines and to generate high quality figures and reports. We also developed PyGNA to take advantage of multi-core systems to generate calibrated null distributions on large datasets. We then present the results of extensive benchmarking of the tests implemented in PyGNA and a use case inspired by RNA sequencing data analysis, showing how PyGNA can be easily integrated to study biological networks. PyGNA is available at http://github.com/stracquadaniolab/pygna and can be easily installed using the PyPi or Anaconda package managers, and Docker.

conclusionsWe present a tool for network-aware geneset analysis. PyGNA can either be readily used and easily integrated into existing high-performance data analysis pipelines or as a Python package to implement new tests and analyses. With the increasing availability of population-scale omic data, PyGNA provides a viable approach for large scale geneset network analysis.

Indexed as

Gene Regulatory NetworksProgramming LanguagesSoftwareAlgorithmsComputer SimulationSequence Analysis, RNAStochastic ProcessesBiological NetworksGeneset Network AnalysisNetwork analysis workflow

Identifiers

PMID33092528
PMCPMC7579948
OpenAlexW3094479861

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.