EDLM: Ensemble Deep Learning Model to Detect Mutation for the Early Detection of Cholangiocarcinoma

Author:

Shah Asghar Ali1,Alturise Fahad2ORCID,Alkhalifah Tamim2ORCID,Faisal Amna3,Khan Yaser Daanial4ORCID

Affiliation:

1. Department of Computer Science, Bahria University, Islamabad 04408, Pakistan

2. Department of Computer, College of Science and Arts in Ar Rass, Qassim University, Ar Rass 51921, Qassim, Saudi Arabia

3. Department of Computer Science, Bahria University, Lahore 54782, Pakistan

4. Department of Computer Science, University of Management and Technology, Lahore 54782, Pakistan

Abstract

The most common cause of mortality and disability globally right now is cholangiocarcinoma, one of the worst forms of cancer that may affect people. When cholangiocarcinoma develops, the DNA of the bile duct cells is altered. Cholangiocarcinoma claims the lives of about 7000 individuals annually. Women pass away less often than men. Asians have the greatest fatality rate. Following Whites (20%) and Asians (22%), African Americans (45%) saw the greatest increase in cholangiocarcinoma mortality between 2021 and 2022. For instance, 60–70% of cholangiocarcinoma patients have local infiltration or distant metastases, which makes them unable to receive a curative surgical procedure. Across the board, the median survival time is less than a year. Many researchers work hard to detect cholangiocarcinoma, but this is after the appearance of symptoms, which is late detection. If cholangiocarcinoma progression is detected at an earlier stage, then it will help doctors and patients in treatment. Therefore, an ensemble deep learning model (EDLM), which consists of three deep learning algorithms—long short-term model (LSTM), gated recurrent units (GRUs), and bi-directional LSTM (BLSTM)—is developed for the early identification of cholangiocarcinoma. Several tests are presented, such as a 10-fold cross-validation test (10-FCVT), an independent set test (IST), and a self-consistency test (SCT). Several statistical techniques are used to evaluate the proposed model, such as accuracy (Acc), sensitivity (Sn), specificity (Sp), and Matthew’s correlation coefficient (MCC). There are 672 mutations in 45 distinct cholangiocarcinoma genes among the 516 human samples included in the proposed study. The IST has the highest Acc at 98%, outperforming all other validation approaches.

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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