BioData Mining

Announcing our new Aims & Scope!

We are excited to announce that our Aims & Scope has undergone some changes, incorporating an encouragement of submissions pertaining to Artificial Intelligence, Machine Learning, and Visual Analytics, and expanding the data types we consider, to include imaging, electronic health records, biobanks, environmental data, social and behavioral data, wearable devices, and social media data. Please click here to check out the new Aims & Scope and types of submissions that we readily encourage you to submit.

Call for Papers: Integrative Analysis of Multi-Omics Data for Precision Medicine

We are calling for submissions to our new Collection focusing on the development, evaluation, and application of innovative approaches that bridge genomics, transcriptomics, proteomics, metabolomics, and other omics domains, ultimately paving the way for a deeper understanding of disease mechanisms and the development of personalized therapeutic strategies.

Call for Papers: Machine Learning Approaches for Early Diagnosis of Alzheimer’s Disease

We are calling for submissions to our new Collection which will focus on the development, evaluation, and application of new artificial intelligence methods and software for the analysis of Alzheimer’s disease data.

Featured series: Next-generation machine learning

Our new thematic series, edited by Jason Moore and Marylyn Ritchie, seeks manuscripts on the topic of machine learning. We are interested in both original research and review papers, especially those that address new and novel machine learning methods and their application to biological and biomedical big data. The series is open, and you can find out more about it (including submission instructions), here.

The Biomedical Informatics Roundtable Podcast

We are happy to announce that our Editors-in-Chief, Jason H. Moore and Marylyn D. Ritchie, have recently launched a podcast! The Biomedical Informatics Roundtable Podcast aims to bring you discussion of hot topics, recent papers, news, conferences, open data, open-source software, and advice for trainees as well as interviews and spotlights biomedical informatics colleagues from around the world. Please check out Dr Moore and Dr Ritchie’s podcast, here!

Editors' profiles

Dr Jason Moore is the Edward Rose Professor of Informatics, Professor of Biostatistics and Epidemiology, and Professor of Genetics at the Perelman School of Medicine of the University of Pennsylvania. He serves as the first permanent Director of the Institute for Biomedical Informatics and founding Director of the Division of Informatics in the Department of Biostatistics and Epidemiology. He also serves as Senior Associate Dean for Informatics. His work has been communicated in more than 400 scientific publications and he serves as PI on several NIH R01 grants. He has been recognized as a national leader in informatics through election as a Fellow of the American Association for the Advancement of Sciences (AAAS) and as a Kavli Fellow of the National Academy of Sciences (NAS). He was recently elected a Fellow of the American College of Medical Informatics (ACMI).

Marylyn D. Ritchie, PhD is a Professor in Genetics, Director of the Center for Translational Bioinformatics, and Associate Director for Bioinformatics in the Institute for Biomedical Informatics at the University of Pennsylvania School of Medicine.  Dr. Ritchie is a computational geneticist and biomedical informatician with a focus on detecting disease-susceptibility genes associated with common, complex human disease and integrating electronic health records with genomics. She has expertise in developing novel bioinformatics tools for complex analysis of big data in genetics, genomics, and clinical databases, in particular in the area of Pharmacogenomics.  Some of her methods include Multifactor Dimensionality Reduction (MDR), the Analysis Tool for Heritable and Environmental Network Associations (ATHENA), and the Biosoftware suite for annotating/ filtering variants and genomic regions as well as building models of biological relevance for gene-gene interactions and rare-variant burden/dispersion tests.  Dr. Ritchie has over 15 years of experience in the analysis of complex data and has authored over 300 publications (H-index 76).  She is one of Thomas Reuters Most Highly Cited Researchers for 2014.  Dr. Ritchie has extensive experience in leading large collaborative efforts; has been a part of national networks using electronic health records and genomics data; has excellent organizational and leadership skills.  Dr. Ritchie is well suited to be a collaborator on this project.