Evidence map›Paper›PMID 26342102›Full record

ArticleBioinformatics (Oxford, England)2015

Deciphering the associations between gene expression and copy number alteration using a sparse double Laplacian shrinkage approach.

Xingjie Shi, Qing Zhao, Jian Huang, Yang Xie, Shuangge Ma

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  4. Review
  5. Integration of Proteomics and Other Omics Data.Methods in molecular biology (Clifton, N.J.) · 2021
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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

5 authors.

Xingjie ShiDepartment of Statistics, Nanjing University of Finance and Economics, Nanjing, China, School of Statistics and Management, Shanghai University of Finance and Economics, Shanghai, China.
Qing ZhaoDepartment of Biostatistics, Yale University, New Haven, CT, USA.
Jian HuangDepartment of Statistics and Actuarial Science, University of Iowa, Iowa, IA, USA.
Yang XieDepartment of Clinical Science, The University of Texas Southwestern Medical Center, Dallas, TX, USA and.
Shuangge MaDepartment of Biostatistics, Yale University, New Haven, CT, USA, VA Cooperative Studies Program Coordinating Center, West Haven, CT, USA.

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI DAVID F STERN · 2006 to 2026
$43.9M
Novel Methods for Integrative Analysis of Cancer Genomic DataR01CA142774 · NCI · YALE UNIVERSITY · PI MA, SHUANGGE · 2010 to 2013
$1.3M
Development of Integrated Analysis Methods and Applications to TCGA dataR03CA182984 · NCI · YALE UNIVERSITY · PI MA, SHUANGGE · 2014 to 2015
$167k
NCI NIH HHS CA142774NCI NIH HHS CA182984NCI NIH HHS P30CA016359NCI NIH HHS P50 CA121974NCI NIH HHS P50CA121974NCI NIH HHS R03 CA182984
6 · The paper itself

Abstract

motivationBoth gene expression levels (GEs) and copy number alterations (CNAs) have important biological implications. GEs are partly regulated by CNAs, and much effort has been devoted to understanding their relations. The regulation analysis is challenging with one gene expression possibly regulated by multiple CNAs and one CNA potentially regulating the expressions of multiple genes. The correlations among GEs and among CNAs make the analysis even more complicated. The existing methods have limitations and cannot comprehensively describe the regulation.

resultsA sparse double Laplacian shrinkage method is developed. It jointly models the effects of multiple CNAs on multiple GEs. Penalization is adopted to achieve sparsity and identify the regulation relationships. Network adjacency is computed to describe the interconnections among GEs and among CNAs. Two Laplacian shrinkage penalties are imposed to accommodate the network adjacency measures. Simulation shows that the proposed method outperforms the competing alternatives with more accurate marker identification. The Cancer Genome Atlas data are analysed to further demonstrate advantages of the proposed method. AVAILABILITY AND IMPLEMENTATION: R code is available at http://works.bepress.com/shuangge/49/.

Indexed as

Gene DosageGene ExpressionGene Expression RegulationModels, TheoreticalHumansNeoplasms

Identifiers

PMID26342102
PMCPMC5013934

What OpenQuestion holds

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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.