Evidence map›Paper›PMID 31653243›Full record

ArticleBMC cancer2019

lionessR: single sample network inference in R.

Marieke L Kuijjer, Ping-Han Hsieh, John Quackenbush, Kimberly Glass

Abstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

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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

4 authors.

Marieke L KuijjerCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, Gaustadalléen 21, Oslo, 0318, Norway. marieke.kuijjer@ncmm.uio.no.ORCID http://orcid.org/0000-0001-6280-3130
Ping-Han HsiehCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, Gaustadalléen 21, Oslo, 0318, Norway.
John QuackenbushDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, 677 Huntington Ave, Boston, 02215, USA.
Kimberly GlassChanning Division of Network Medicine, Brigham and Women's Hospital, 181 Longwood Avenue, Boston, 02215, USA.

Funding

Systems Biology, Bioinformatics, and BiostatisticsP01HL105339 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SILVERMAN, EDWIN K · 2011 to 2015
$12.2M
Unraveling the Complexities of Risk and Mechanism in CancerR35CA220523 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI QUACKENBUSH, JOHN · 2018 to 2024
$6.0M
Using Networks to Assign Gene Function in Lung DiseaseR01HL111759 · NHLBI · DANA-FARBER CANCER INST · PI QUACKENBUSH, JOHN, SILVERMAN, EDWIN K · 2012 to 2015
$3.4M
Using Integrative Networks to Explore Heterogeneous Phenotypes in COPDK25HL133599 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI GLASS, KIMBERLY RENEE · 2016 to 2020
$945k
NCI NIH HHS 1R35CA220523NCI NIH HHS R35 CA220523NHLBI NIH HHS K25 HL133599NHLBI NIH HHS K25HL133599NHLBI NIH HHS P01 HL105339NHLBI NIH HHS P01HL105339NHLBI NIH HHS R01 HL111759NHLBI NIH HHS R01HL111759
6 · The paper itself

Abstract

backgroundIn biomedical research, network inference algorithms are typically used to infer complex association patterns between biological entities, such as between genes or proteins, using data from a population. This resulting aggregate network, in essence, averages over the networks of those individuals in the population. LIONESS (Linear Interpolation to Obtain Network Estimates for Single Samples) is a method that can be used together with a network inference algorithm to extract networks for individual samples in a population. The method's key characteristic is that, by modeling networks for individual samples in a data set, it can capture network heterogeneity in a population. LIONESS was originally made available as a function within the PANDA (Passing Attributes between Networks for Data Assimilation) regulatory network reconstruction framework. However, the LIONESS algorithm is generalizable and can be used to model single sample networks based on a wide range of network inference algorithms.

resultsIn this software article, we describe lionessR, an R implementation of LIONESS that can be applied to any network inference method in R that outputs a complete, weighted adjacency matrix. As an example, we provide a vignette of an application of lionessR to model single sample networks based on correlated gene expression in a bone cancer dataset. We show how the tool can be used to identify differential patterns of correlation between two groups of patients.

conclusionsWe developed lionessR, an open source R package to model single sample networks. We show how lionessR can be used to inform us on potential precision medicine applications in cancer. The lionessR package is a user-friendly tool to perform such analyses. The package, which includes a vignette describing the application, is freely available at: https://github.com/kuijjerlab/lionessR and at: http://bioconductor.org/packages/lionessR .

Indexed as

AlgorithmsComputer SimulationSoftwareBiopsyBone NeoplasmsComputational BiologyGene Regulatory NetworksHumansNeoplasmsOsteosarcomaPrecision MedicineSurvival AnalysisTranscriptomeAlgorithmsBiological networksCo-expressionComputational biologyGene regulationNetwork analysisOsteosarcomaPrecision medicineSoftware tools

Identifiers

PMID31653243
PMCPMC6815019

What OpenQuestion holds

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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.