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Maani, N.

Publications and source records attributed to Maani, N..

2 recordsLinked to original sources

Visible neural networks for multi-omics integration: a critical review

Biomarker discovery and drug response prediction is central to personalized medicine, driving demand for predictive models that also offer biological insights. Biologically informed neural networks (BINNs), also known as visible neural networks (VNNs), have recently emerged as a solution to this goal. BINNs or VNNs are neural networks whose inter-layer connections are constrained based on prior knowledge from gene on-tologies pathway databases. These sparse models enhance interpretability by embedding prior knowledge into their architecture, ideally reducing the space of learnable functions to those that are biologically meaningful. In this systematic review--the first of its kind-- we identify 86 recent papers implementing such models and highlight key trends in architectural design decisions, data sources and methods for evaluation. Growth in popularity of the approach is apparently mitigated by a lack of standardized terminology, tools and benchmarks.

bioinformatics↗

Natural history of a mouse model of X-linked myotubular myopathy

X-linked myotubular myopathy is a severe monogenetic disorder of the skeletal muscle caused by loss of expression/function mutations in the MTM1 (myotubularin) gene. There is a growing understanding of the pathologic and molecular abnormalities associated with loss of MTM1, and emerging therapeutic strategies that are in the process of translation to patients. Much of these data have been uncovered through experimentation in pre-clinical animal models of the disease. The most widely used model is an Mtm1 gene knockout mouse line; this line faithfully recapitulates the salient genetic and pathologic features of the disease. Despite the advances in aspects of XLMTM, there remain many unknowns related to disease pathomechanisms and to understanding of MTM1s function in normal muscle development, and a continued need for therapy identification and development. To address these barriers, and to lay the groundwork for future study, we performed a natural history study of the Mtm1 knockout mouse model of XLMTM. We show that certain molecular and pathologic changes precede overt phenotypic changes, while others, including abnormalities in triad structure, occur more coincident with muscle weakness in the mouse. In total, we provide a comprehensive longitudinal assessment of molecular and structural features of the murine XLMTM disease process.

genetics↗