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Allmer, J.

Publications and source records attributed to Allmer, J..

3 recordsLinked to original sources

G-S-M: A Comprehensive Framework for Integrative Feature Selection in Omics Data Analysis and Beyond

The treatment of human diseases is a major research question in many fields related to medicine. It has become clear that patient stratification is of utmost importance so that patients receive the best possible treatment. Bio/disease markers are critical to achieve stratification. Markers can come from many different sources such as genomics, transcriptomics, and proteomics. Establishing markers from such measurements often involves data analysis, machine learning, and feature selection. Traditional feature selection techniques often rely on the estimation of individual feature importance or significance by assigning a score to each feature, disregarding the inter-feature relationships. In contrast, the G-S-M (grouping scoring modeling) approach considers a group of features as a set that is organized based on prior knowledge. This approach takes into account the interdependence among features, providing a more meaningful evaluation of feature relevance and utility. Prior knowledge can encompass much compiled information such as microRNA-target interactions and protein-protein interactions. Here we present a new tool called G-S-M that presents the generalization of our previous works such as maTE, CogNet, and PriPath. The G-S-M tool combines machine learning and prior knowledge to group and score features based on their association with a binary-labeled target such as control and disease. This approach is unique in that computational and domain knowledge is utilized concurrently. Embedded feature selection, repeatedly employing machine learning during the selection process results in the identification of the most discriminative groups. Furthermore, the G-S-M tool allows for a more holistic understanding of the underlying mechanisms of a given system to be achieved through the combination of machine learning and prior domain knowledge, which can lead to new insights and discoveries. The implementation of the G-S-M workflow is freely available for download from our GitHub repository: https://github.com/malikyousef/The-G-S-M-Grouping-Scoring-Modeling-Approach. With this generalized approach we aim to make the feature selection approach available to a broader audience and hope it will be employed in medical practice. An example of such an approach is the TextNetTopics that is based on the G-S-M approach. TextNetTopics uses Latent Dirichlet Allocation (LDA) to detect topics of words, where those topics serve as groups. In the future, we aim to extend the approach to enable the incorporation of multiple lines of evidence for biomarker detection and patient stratification via combining multi-omics data.

bioinformatics↗

Detection of pre-microRNA with Convolutional Neural Networks

MicroRNAs (miRNAs) are small non-coding RNA sequences that have been implicated in many physiological processes and diseases. The experimental discovery of miRNAs is complicated because both miRNAs and their targets need to be expressed for the confirmation of functional interactions, but expression is under spatiotemporal control. This has motivated the development of computational methods for miRNA detection. This typically involves feature design by domain experts followed by machine learning. While handcrafted features can encode domain knowledge, feature engineering is a time-consuming task. Additionally, some of the currently most successful features for pre-miRNA detection, such as p-value based ones, require comparably large computations. In contrast, advances of representation learning methods such as deep learning can discover relevant features directly from data. Here, we propose a method that uses domain knowledge to create an efficient graphical representation of pre-miRNAs, encoding sequence, structure, and implicitly some thermodynamic information. A suitable convolutional neural network architecture for pre-miRNA detection was used to train a model. This model achieves state-of-the-art performance on all previously used datasets. Additionally, computations succeed in real time thereby overcoming current speed limitations. Finally, our strategy promises future interpretability of the trained models and in turn novel biological interpretations of pre-miRNA characteristics.

bioinformatics↗

Boron Hyperaccumulation Mechanisms in Puccinellia distans as Revealed by Transcriptomic Analysis

Boron is an essential plant micronutrient; but is toxic at high concentrations. Boron toxicity can severely affect crop productivity in arid and semi-arid environments. Puccinellia distans (Jacq.) Par1., common alkali grass, is found throughout the world and can survive under boron concentrations that are lethal for other plant species. In addition, P. distans can accumulate very high levels of this element. Despite these interesting features, very little research has been performed to elucidate the boron tolerance mechanism in this species. In this study, P. distans samples were analyzed by RNA sequencing to identify genes related to boron tolerance and hyperaccumulation. Abundance levels of selected differentially expressed transcripts were validated by real-time PCR. The results indicated that the hyperaccumulation mechanism of P. distans involves many transcriptomic changes including those that lead to: alterations in the malate pathway, changes in cell wall components that allow sequestration of excess boron without toxic effects, and increased expression of at least one putative boron transporter and two putative aquaporins. Elucidation of the boron accumulation mechanism is important to develop approaches for bioremediation of boron contaminated soils.

plant biology↗