Evidence map›Paper›PMID 34377946›Full record

ArticleJournal of bioinformatics and genomics2016

A two-stage approach for combining gene expression and mutation with clinical data improves survival prediction in myelodysplastic syndromes and ovarian cancer.

Yan Li, Xinyan Zhang, Tomi Akinyemiju, Akinyemi I Ojesina, Jeff M Szychowski, Nianjun Liu, Bo Xu, Nengjun Yi

Abstract read
In one paragraph

Article in Journal of bioinformatics and genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yan LiDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Xinyan ZhangDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Tomi AkinyemijuDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Akinyemi I OjesinaDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Jeff M SzychowskiDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Nianjun LiuDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Bo XuDepartment of Oncology, Southern Research Institute, Birmingham, AL 35205, USA.
Nengjun YiDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Funding

National Dissemination of I-Corps@NCATS: Accelerating Translation through CommercializationUL1TR003096 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GUTIERREZ, ORLANDO M, KIMBERLY, ROBERT P. · 2019 to 2023
$43.6M
UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
UAB Multidisciplinary Clinical Research CenterP60AR064172 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRIDGES, S LOUIS · 2013 to 2018
$4.5M
Bayesian Methods for Mapping Complex Epistatic GenesR01GM069430 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YI, NENGJUN · 2005 to 2013
$2.3M
Genome Wide Haplotype Association AnalysisR01GM081488 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, NIANJUN · 2008 to 2012
$1.3M
Secondary analysis and risk prediction of dental caries and oral cleftsR03DE024198 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, NIANJUN · 2015 to 2016
$456k
NCATS NIH HHS UL1 TR001417NCATS NIH HHS UL1 TR003096NIAMS NIH HHS P60 AR064172NIDCR NIH HHS R03 DE024198NIGMS NIH HHS R01 GM069430NIGMS NIH HHS R01 GM081488
6 · The paper itself

Abstract

motivationMany traditional clinical prognostic factors have been known for cancer for years, but usually provide poor survival prediction. Genomic information is more easily available now which offers opportunities to build more accurate prognostic models. The challenge is how to integrate them to improve survival prediction. The common approach of jointly analyzing all type of covariates directly in one single model may not improve the prediction due to increased model complexity and cannot be easily applied to different datasets.

resultsWe proposed a two-stage procedure to better combine different sources of information for survival prediction, and applied the two-stage procedure in two cancer datasets: myelodysplastic syndromes (MDS) and ovarian cancer. Our analysis suggests that the prediction performance of different data types are very different, and combining clinical, gene expression and mutation data using the two-stage procedure improves survival prediction in terms of improved concordance index and reduced prediction error. AVAILABILITY AND IMPLEMENTATION: The two-stage procedure can be implemented in BhGLM package which is freely available at http://www.ssg.uab.edu/bhglm/. CONTACT: nyi@uab.edu.

Identifiers

PMID34377946
PMCPMC8351588

What OpenQuestion holds

Textmetadata
LicenceTDM
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.