Evidence map›Paper›PMID 40221543›Full record

ArticleScientific reports2025

Double weighted k nearest neighbours for binary classification of high dimensional genomic data.

Amjad Ali, Zardad Khan, Hailiang Du, Saeed Aldahmani

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

4 authors.

Amjad AliDepartment of Statistics and Bussines Analytics, United Arab Emirates University, Al Ain, United Arab Emirates.
Zardad KhanDepartment of Statistics and Bussines Analytics, United Arab Emirates University, Al Ain, United Arab Emirates. zaar@uaeu.ac.ae.
Hailiang DuDepartment of Mathematical Sciences, Durham University, Stockton Rd, Durham, UK.
Saeed AldahmaniDepartment of Statistics and Bussines Analytics, United Arab Emirates University, Al Ain, United Arab Emirates. saldahmani@uaeu.ac.ae.

Funding

United Arab Emirates University 12B041
6 · The paper itself

Abstract

High dimensional gene expression datasets consist of a large number of genes, many of which do not play a significant role in classifying tissue samples. The high dimensional nature of this type of data, characterized by a large number of gene features substantially exceeding its sample size, makes it challenging for existing methods to work efficiently in terms of prediction accuracy and execution time. To address this issue, a new classification procedure called double weighted k nearest neighbours ([Formula: see text]) is proposed. [Formula: see text] is specifically designed for gene expression data and incorporates feature weights derived from genes' ability to express deferentially between classes. Features weights are derived in a manner that automatically increase the impact of informative features while decreasing it for features that are less/non informative. To achieve this goal, the estimated weighted distances from the observations in the k nearest neighbourhood to the test point are used in an exponential function. The outputs of the function are summed for both the classes separately and the test point is assigned the class label with the largest sum. By utilizing the proposed weighting method based on the differential capability of genes, the [Formula: see text] method aims to achieve robust and efficient classification by allowing only the most informative features/genes to contribute to the classification task. Experimental evaluations, in comparison with several methods, i.e., standard [Formula: see text], weighted k nearest neighbours classifier ([Formula: see text]), random k nearest neighbour ([Formula: see text]), extended neighbourhood rule ensemble (ExNRule), k conditional nearest neighbour ([Formula: see text]), [Formula: see text] ensemble and support vector machines (SVM), demonstrate the effectiveness of [Formula: see text] in accurately classifying gene expression datasets. Overall, [Formula: see text] presents a promising approach for gene expression data analysis through the two fold weighted distance calculation strategy using classification accuracy, Cohen's kappa, sensitivity and [Formula: see text]score as performance metrics.

Indexed as

Gene Expression ProfilingGenomicsAlgorithmsComputational BiologyDatabases, GeneticHumans

Identifiers

PMID40221543
PMCPMC11993671

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.