Evidence map›Paper›PMID 36411295›Full record

ArticleScientific reports2022

Prediction of [Formula: see text]-Thalassemia carriers using complete blood count features.

Furqan Rustam, Imran Ashraf, Shehbaz Jabbar, Kilian Tutusaus, Cristina Mazas, Alina Eugenia Pascual Barrera, Isabel de la Torre Diez

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Diagnosis and classification of thalassemia disease using machine learning: Comparative analysis of traditional models and a novel hybrid approach.Technology and health care : official journal of the European Society for Engineering and Medicine · 2026
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  2. Prediction ofFrontiers in medicine · 2026
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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

7 authors at 7 institutions in 4 countries.

Furqan RustamFaculty of Computer Science and Information Technology, Khwaja Fareed University of Engineering and Information Technology, Rahim Yar Khan, Pakistan.
Imran AshrafInformation and Communication Engineering, Yeungnam University, Gyeongsan, 38541 Korea.
Shehbaz JabbarSheikh Zayed Hospital and Medical College, Rahim Yar Khan, 64200 Pakistan.
Kilian TutusausUniversidad Europea del Atlántico, Isabel Torres 21, 39011 Santander, Spain.
Cristina MazasUniversidad Europea del Atlántico, Isabel Torres 21, 39011 Santander, Spain.
Alina Eugenia Pascual BarreraUniversidad Europea del Atlántico, Isabel Torres 21, 39011 Santander, Spain.
Isabel de la Torre DiezDepartment of Signal Theory and Communications and Telematic Engineering, University of Valladolid, Paseo de Belén 15, 47011 Valladolid, Spain.
Fundación Universitaria Internacional de ColombiaKhwaja Fareed University of Engineering and Information Technology · PKShaikh Zayed Medical College and Hospital · PKUniversidad de Valladolid · ESUniversidad Europea del Atlántico · ESUniversidad Internacional · MXYeungnam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[Formula: see text]-Thalassemia is one of the dangerous causes of the high mortality rate in the Mediterranean countries. Substantial resources are required to save a [Formula: see text]-Thalassemia carriers' life and early detection of thalassemia patients can help appropriate treatment to increase the carrier's life expectancy. Being a genetic disease, it can not be prevented however the analysis of several indicators in parents' blood can be used to detect disorders causing Thalassemia. Laboratory tests for Thalassemia are time-consuming and expensive like high-performance liquid chromatography, Complete Blood Count (CBC) with peripheral smear, genetic test, etc. Red blood indices from CBC can be used with machine learning models for the same task. Despite the available approaches for Thalassemia carriers from CBC data, gaps exist between the desired and achieved accuracy. Moreover, the data imbalance problem is studied well which makes the models less generalizable. This study proposes a highly accurate approach for [Formula: see text]-Thalassemia detection using red blood indices from CBC augmented by supervised machine learning. In view of the fact that all the features do not carry predictive information regarding the target variable, this study employs a unified framework of two features selection techniques including Principal Component Analysis (PCA) and Singular Vector Decomposition (SVD). The data imbalance between [Formula: see text]-Thalassemia carrier and non-carriers is handled by Synthetic Minority Oversampling Technique (SMOTE) and Adaptive Synthetic (ADASYN). Extensive experiments are performed using many state-of-the-art machine learning models and deep learning models. Experimental results indicate the superiority of the proposed approach over existing approaches with an accuracy score of 0.96.

Indexed as

ThalassemiaAlgorithmsAnimalsBlood Cell CountChromatography, High Pressure LiquidDisease VectorsHumans

Identifiers

PMID36411295
PMCPMC9678892
OpenAlexW4309495846

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.