GenomicsKG: A Knowledge Graph to Visualize Poly-Omics Data

Jha, Alokkumar; d’Aquin, Mathieu; Sahay, Ratnesh; Zehra, Durre; Dangwal, Seema; Khan, Yasar; Mehmood, Qaiser; Rebholz‐Schuhmann, Dietrich; Verma, Ghanshyam

doi:10.3724/sp.j.2640-8686.2019.0063

Cited by 1 publication

(1 citation statement)

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“…Researchers are exploring new ways to use the knowledge represented by biomedical KBs to solve complex problems in the biomedical domain [ 24 – 27 ]. Bonner et al [ 28 ] provide an overview of existing biomedical KBs.…”

Section: Introductionmentioning

confidence: 99%

Enabling personalised disease diagnosis by combining a patient’s time-specific gene expression profile with a biomedical knowledge base

Verma,

Rebholz-Schuhmann,

Madden

2024

BMC Bioinformatics

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Background Recent developments in the domain of biomedical knowledge bases (KBs) open up new ways to exploit biomedical knowledge that is available in the form of KBs. Significant work has been done in the direction of biomedical KB creation and KB completion, specifically, those having gene-disease associations and other related entities. However, the use of such biomedical KBs in combination with patients’ temporal clinical data still largely remains unexplored, but has the potential to immensely benefit medical diagnostic decision support systems. Results We propose two new algorithms, LOADDx and SCADDx, to combine a patient’s gene expression data with gene-disease association and other related information available in the form of a KB, to assist personalized disease diagnosis. We have tested both of the algorithms on two KBs and on four real-world gene expression datasets of respiratory viral infection caused by Influenza-like viruses of 19 subtypes. We also compare the performance of proposed algorithms with that of five existing state-of-the-art machine learning algorithms (k-NN, Random Forest, XGBoost, Linear SVM, and SVM with RBF Kernel) using two validation approaches: LOOCV and a single internal validation set. Both SCADDx and LOADDx outperform the existing algorithms when evaluated with both validation approaches. SCADDx is able to detect infections with up to 100% accuracy in the cases of Datasets 2 and 3. Overall, SCADDx and LOADDx are able to detect an infection within 72 h of infection with 91.38% and 92.66% average accuracy respectively considering all four datasets, whereas XGBoost, which performed best among the existing machine learning algorithms, can detect the infection with only 86.43% accuracy on an average. Conclusions We demonstrate how our novel idea of using the most and least differentially expressed genes in combination with a KB can enable identification of the diseases that a patient is most likely to have at a particular time, from a KB with thousands of diseases. Moreover, the proposed algorithms can provide a short ranked list of the most likely diseases for each patient along with their most affected genes, and other entities linked with them in the KB, which can support health care professionals in their decision-making.

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Section: Introductionmentioning

confidence: 99%