Feature Papers in Computational Biology and Medicine
A special issue of BioMedInformatics (ISSN 2673-7426). This special issue belongs to the section "Computational Biology and Medicine".
Deadline for manuscript submissions: closed (31 January 2024) | Viewed by 37929
Special Issue Editor
Interests: genome medicine; computational biology; genomic regulation
Special Issues, Collections and Topics in MDPI journals
Special Issue Information
Dear Colleagues,
Multiomics diagnostics for cancer
Multi-omics high-throughput technologies are producing a steeply increasing number of data sets, which are not restricted to only one but consist of multiple omics modalities extracted from the same samples (e.g., in patient-matched tumor specimens). These data offer tremendous opportunities for enhancing our molecular understanding of biological systems, particularly regarding different but mutually linked layers of genomic regulation, usually subsumed as the basic “omes”—genome, epigenome, transcriptome, proteome and metabolome. The joint, integrative analysis of these omics modalities and the development of appropriate computational methods is essential to obtain a comprehensive overview of the otherwise fragmented information hidden in this data. The molecular pathomechanisms of cancer are often driven by a complex interplay between the omes, including genetic defects, epigenetic reprogramming, and perturbed transcription factor networks. Practical objectives of computational methods are the description of cancer heterogeneity in terms of subtypes and the extraction of prognostic markers from the different “omes”, for example, by asking whether single omics modalities or combinations of them are better suited and if so, what modality is “the best” or how to combine them optimally. The Special Issue aims to address a wide scope of areas related to cancer diagnostics, ranging from computational methods integrating different omes (e.g., for subtyping cancer heterogeneity, their prognosis and personalization), to applications to different cancer types and omics realms (genetics, transcriptomics, epigenetics, metabolomics, proteomics) and their associations with clinical data.
Understanding Pathomechanisms in the single-cell omics era
Single-cell sequencing technologies are revolutionizing our view of biological systems across several research fields by illuminating the complex cell type and state landscape. They make it possible to understand cancer as an evolving cellular disease, provide new details of aberrant cellular functions of neurodegenerative diseases, decipher the diversity of immune cells and their interactions in the tumor microenvironment, pathomechanisms of autoimmunity and inflammatory diseases with single-immune-cell resolution, and provide new insights into a series of other complex and/or rare diseases. This Special Issue will collect methods and applications of single-cell omics analytics, primarily transcriptomics but also chromatin accessibility (ATAC) and other omics applications, and, as an option, their combination with bulk omics data. The central objective is to learn about the particular benefit of the cellular view for the understanding of pathomechanisms and potential treatment options.
Dr. Hans Binder
Guest Editor
Manuscript Submission Information
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Keywords
- multiomics diagnostics for cancer
- understanding patho mechanisms in the era of single cell transcriptomics
- systems biology of drug repurposing
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