Evidence map›Paper›PMID 30081434›Full record

ArticleBiometrics2019

Joint skeleton estimation of multiple directed acyclic graphs for heterogeneous population.

Jianyu Liu, Wei Sun, Yufeng Liu

Abstract read
In one paragraph

Article in Biometrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Jianyu LiuDepartment of Statistics and Operations Research, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, U.S.A.
Wei SunBiostatistics Program, Public Health Sciences Division Fred Hutchinson Cancer Research Center, Seattle, Washington, U.S.A.ORCID 0000-0002-6350-1107
Yufeng LiuDepartment of Statistics and Operations Research, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, U.S.A.ORCID 0000-0002-1686-0545

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Statistical Methods for RNA-seq Data AnalysisR01GM105785 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Wei Sun · 2014 to 2026
$4.6M
Statistical Methods for Analysis of Tumor Heterogeneity in Genetic EpidemiologyR01CA189532 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HSU, LI · 2015 to 2023
$4.2M
Unlocking complex co-expression network using graphical modelsR01GM126550 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, YUFENG · 2017 to 2020
$1.6M
NCI NIH HHS P01 CA142538NCI NIH HHS R01 CA189532NIGMS NIH HHS R01 GM105785NIGMS NIH HHS R01 GM126550
6 · The paper itself

Abstract

The directed acyclic graph (DAG) is a powerful tool to model the interactions of high-dimensional variables. While estimating edge directions in a DAG often requires interventional data, one can estimate the skeleton of a DAG (i.e., an undirected graph formed by removing the direction of each edge in a DAG) using observational data. In real data analyses, the samples of the high-dimensional variables may be collected from a mixture of multiple populations. Each population has its own DAG while the DAGs across populations may have significant overlap. In this article, we propose a two-step approach to jointly estimate the DAG skeletons of multiple populations while the population origin of each sample may or may not be labeled. In particular, our method allows a probabilistic soft label for each sample, which can be easily computed and often leads to more accurate skeleton estimation than hard labels. Compared with separate estimation of skeletons for each population, our method is more accurate and robust to labeling errors. We study the estimation consistency for our method, and demonstrate its performance using simulation studies in different settings. Finally, we apply our method to analyze gene expression data from breast cancer patients of multiple cancer subtypes.

Indexed as

Epidemiologic Research DesignModels, StatisticalBreast NeoplasmsComputer GraphicsComputer SimulationFemaleGene ExpressionGenes, NeoplasmHumansBi-level selectionDAGPC algorithmProbabilistic labelsSoft classifier

Identifiers

PMID30081434
PMCPMC6546091

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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.