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JMIR Bioinformatics and Biotechnology|May 19, 2023
Exploring the Applicability of Using Natural Language Processing to Support Nationwide Venous Thromboembolism Surveillance: Model Evaluation StudyAaron Wendelboe, Ibrahim Saber, Justin Dvorak, et al.JMIR Bioinformatics and Biotechnology|June 29, 2024
Molecular Docking Using Chimera and Autodock Vina Software for NonbioinformaticiansSania Safdar Butt, Yasmin Badshah, Maria Shabbir, et al.JMIR Bioinformatics and Biotechnology|October 16, 2024
Internet-Based Abnormal Chromosomal Diagnosis During Pregnancy Using a Noninvasive Innovative Approach to Detecting Chromosomal Abnormalities in the Fetus: Scoping ReviewMega Obukohwo Sr Oyovwi, Ejiro Peggy Ohwin, Rume Arientare Rotu, et al.JMIR Bioinformatics and Biotechnology|April 10, 2025
Decentralized Biobanking Apps for Patient Tracking of Biospecimen Research: Real-World Usability and Feasibility StudyWilliam Sanchez, Ananya Dewan, Eve Budd, et al.JMIR Bioinformatics and Biotechnology|March 13, 2025
A Hybrid Deep Learning-Based Feature Selection Approach for Supporting Early Detection of Long-Term Behavioral Outcomes in Survivors of Cancer: Cross-Sectional StudyTracy Huang, Chun-Kit Ngan, Yin Ting Cheung, et al.JMIR Bioinformatics and Biotechnology|June 27, 2024
It Is in Our DNA: Bringing Electronic Health Records and Genomic Data Together for Precision MedicineAlan J Robertson, Andrew J Mallett, Zornitza Stark, et al.JMIR Bioinformatics and Biotechnology|June 27, 2024
Reducing Crowding in Emergency Departments With Early Prediction of Hospital Admission of Adult Patients Using Biomarkers Collected at Triage: Retrospective Cohort StudyAnn Corneille Monahan, Sue S Feldman, Tony P FitzgeraldJMIR Bioinformatics and Biotechnology|June 27, 2024
Mutational Patterns Observed in SARS-CoV-2 Genomes Sampled From Successive Epochs Delimited by Major Public Health Events in Ontario, Canada: Genomic Surveillance StudyDavid Chen, Gurjit S Randhawa, Maximillian Pm Soltysiak, et al.JMIR Bioinformatics and Biotechnology|June 27, 2024
Diagnosis of a Single-Nucleotide Variant in Whole-Exome Sequencing Data for Patients With Inherited Diseases: Machine Learning Study Using Artificial Intelligence Variant PrioritizationYu-Shan Huang, Ching Hsu, Yu-Chang Chune, et al.JMIR Bioinformatics and Biotechnology|July 24, 2024
Deep Learning-Based Identification of Tissue of Origin for Carcinomas of Unknown Primary Using MicroRNA Expression: Algorithm Development and ValidationAnanya Raghu, Anisha Raghu, Jillian F WisePageof 9