Evidence map›Paper›PMID 32127576›Full record

ArticleScientific reports2020

HDMAC: A Web-Based Interactive Program for High-Dimensional Analysis of Molecular Alterations in Cancer.

Chung Chang, Chan-Yu Sung, Han Hsiao, Jiabin Chen, I-Hsuan Chen, Wei-Ting Kuo, Lung-Feng Cheng, Praveen Kumar Korla, Ming-Jhe Chung, Pei-Jhen Wu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 41% of its field
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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

12 authors at 3 institutions in 1 country.

Chung ChangDepartment of Applied Mathematics, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.
Chan-Yu SungDepartment of Applied Mathematics, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.
Han HsiaoDepartment of Applied Mathematics, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.
Jiabin ChenInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.ORCID http://orcid.org/0000-0002-6859-4293
I-Hsuan ChenDivision of Transplant Surgery/Urology, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, 81362, Taiwan, ROC.
Wei-Ting KuoDivision of Transplant Surgery/Urology, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, 81362, Taiwan, ROC.
Lung-Feng ChengDivision of Transplant Surgery/Urology, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, 81362, Taiwan, ROC.
Praveen Kumar KorlaInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.
Ming-Jhe ChungDepartment of Applied Mathematics, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.
Pei-Jhen WuDepartment of Applied Mathematics, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.
Chia-Cheng YuDivision of Transplant Surgery/Urology, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, 81362, Taiwan, ROC. tough0857@icloud.com.
Jim Jinn-Chyuan SheuInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC. jimsheu@mail.nsysu.edu.tw.
National Sun Yat-sen University · TWKaohsiung Veterans General Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in high-throughput genomic technologies have nurtured a growing demand for statistical tools to facilitate identification of molecular changes as potential prognostic biomarkers or drugable targets for personalized precision medicine. In this study, we developed a web-based interactive and user-friendly platform for high-dimensional analysis of molecular alterations in cancer (HDMAC) (https://ripsung26.shinyapps.io/rshiny/). On HDMAC, several penalized regression models that are suitable for high-dimensional data analysis, Ridge, Lasso and adaptive Lasso, are offered, with Cox regression for survival and logistic regression for binary outcomes. Choice of a first-step screening is provided to address the multiple-comparison issue that often arises with large-volume genomic data. Hazard ratio or estimated coefficient is provided with each selected gene so that a multivariate regression model may be built based on the genes selected. Cross validation is provided as the method to estimate the prediction power of each regression model. In addition, R codes are also provided to facilitate download of whole sets of molecular variables from TCGA. In this study, illustration of the use of HDMAC was made through a set of data on gene mutations and a set on mRNA expression from ovarian cancer patients and a set on mRNA expression from bladder cancer patient. From the analysis of each set of data, a list of candidate genes was obtained that might be associated with mutations or abnormal expression of genes in ovarian and bladder cancers. HDMAC offers a solution for rigorous and validation analysis of high-dimensional genomic data.

Indexed as

FemaleHumansLogistic ModelsModels, TheoreticalMultivariate AnalysisNeoplasmsOvarian NeoplasmsProportional Hazards ModelsRNA, MessengerRNA, Messenger

Identifiers

PMID32127576
PMCPMC7054321
OpenAlexW3010530498

What OpenQuestion holds

Textmetadata
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.