Evidence map›Paper›PMID 25887568›Full record

ArticleBMC genomics2015

ENCAPP: elastic-net-based prognosis prediction and biomarker discovery for human cancers.

Jishnu Das, Kaitlyn M Gayvert, Florentina Bunea, Marten H Wegkamp, Haiyuan Yu

Abstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  11. Data analysis methods for defining biomarkers from omics data.Analytical and bioanalytical chemistry · 2022
    Review
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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.

Jishnu DasDepartment of Biological Statistics and Computational Biology, Cornell University, 335 Weill Hall, Ithaca, NY, 14853, USA. jd327@cornell.edu.
Kaitlyn M GayvertTri-Institutional Training Program in Computational Biology and Medicine, New York, NY, 10065, USA. kmg257@cornell.edu.
Florentina BuneaDepartment of Statistical Science, Cornell University, Ithaca, NY, 14853, USA. fb238@cornell.edu.
Marten H WegkampDepartment of Statistical Science, Cornell University, Ithaca, NY, 14853, USA. marten.wegkamp@cornell.edu.
Haiyuan YuDepartment of Biological Statistics and Computational Biology, Cornell University, 335 Weill Hall, Ithaca, NY, 14853, USA. haiyuan.yu@cornell.edu.

Funding

Tri-Institutional Training Program in Computational Biology & MedicineT32GM083937 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHRISTINI, DAVID J. · 2009 to 2018
$3.1M
Whole Genome Sequencing to Discover Familial Myeloma Risk GenesR01CA167824 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LIPKIN, STEVEN M, OFFIT, KENNETH · 2012 to 2016
$1.9M
Towards a comprehensive protein interactome network in Schizosaccharomyces pombeR01GM097358 · NIGMS · CORNELL UNIVERSITY · PI YU, HAIYUAN · 2012 to 2016
$1.7M
Using Protein Interactome Networks to Understand the Functional Role of Coding DNR01GM104424 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI LIPKIN, STEVEN M, YU, HAIYUAN · 2013 to 2016
$1.7M
Computational Methods for Unraveling Combinatorial Gene RegulationR01GM108716 · NIGMS · UNIVERSITY OF IOWA · PI TAN, KAI · 2014 to 2017
$1.2M
NCI NIH HHS R01 CA167824NIGMS NIH HHS R01 GM097358NIGMS NIH HHS R01 GM104424NIGMS NIH HHS R01 GM108716NIGMS NIH HHS T32 GM083937NIGMS NIH HHS T32GM083937
6 · The paper itself

Abstract

backgroundWith the explosion of genomic data over the last decade, there has been a tremendous amount of effort to understand the molecular basis of cancer using informatics approaches. However, this has proven to be extremely difficult primarily because of the varied etiology and vast genetic heterogeneity of different cancers and even within the same cancer. One particularly challenging problem is to predict prognostic outcome of the disease for different patients.

resultsHere, we present ENCAPP, an elastic-net-based approach that combines the reference human protein interactome network with gene expression data to accurately predict prognosis for different human cancers. Our method identifies functional modules that are differentially expressed between patients with good and bad prognosis and uses these to fit a regression model that can be used to predict prognosis for breast, colon, rectal, and ovarian cancers. Using this model, ENCAPP can also identify prognostic biomarkers with a high degree of confidence, which can be used to generate downstream mechanistic and therapeutic insights.

conclusionENCAPP is a robust method that can accurately predict prognostic outcome and identify biomarkers for different human cancers.

Indexed as

SoftwareBiomarkers, TumorComputational BiologyGene ExpressionHumansNeoplasmsPrognosisProtein Interaction MapsBiomarkers, Tumor

Identifiers

PMID25887568
PMCPMC4392808

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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.