Evidence map›Paper›PMID 37606439›Full record

ArticleBiotech (Basel (Switzerland))2023

Categorical Data Analysis for High-Dimensional Sparse Gene Expression Data.

Niloufar Dousti Mousavi, Hani Aldirawi, Jie Yang

Abstract read
In one paragraph

Article in Biotech (Basel (Switzerland)), 2023. 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.

Niloufar Dousti MousaviDepartment of Mathematics, Statistics, and Computer Science, University of Illinois at Chicago, Chicago, IL 60607, USA.
Hani AldirawiDepartment of Mathematics, California State University-San Bernardino, San Bernardino, CA 92407, USA.
Jie YangDepartment of Mathematics, Statistics, and Computer Science, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0002-9034-4223

Funding

National Science Foundation DMS-1924859
6 · The paper itself

Abstract

Categorical data analysis becomes challenging when high-dimensional sparse covariates are involved, which is often the case for omics data. We introduce a statistical procedure based on multinomial logistic regression analysis for such scenarios, including variable screening, model selection, order selection for response categories, and variable selection. We perform our procedure on high-dimensional gene expression data with 801 patients, 2426 genes, and five types of cancerous tumors. As a result, we recommend three finalized models: one with 74 genes achieves extremely low cross-entropy loss and zero predictive error rate based on a five-fold cross-validation; and two other models with 31 and 4 genes, respectively, are recommended for prognostic multi-gene signatures.

Indexed as

cross-validationhurdle modelmodel selectionmultinomial logistic modelorder selectionvariable selectionzero-inflated model

Identifiers

PMID37606439
PMCPMC10443356

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.