Sindeeva, M. | Search bioRxiv

bioRxiv2022

PROSTATA: Protein Stability Assessment using Transformers

Accurate prediction of change in protein stability due to point mutations is an attractive goal that remains unachieved. Despite the high interest in this area, little consideration has been given to the transformer architecture, which is dominant in many fields of machine learning. In this work, we introduce PROSTATA, a predictive model built in knowledge transfer fashion on a new curated dataset. PROSTATA demonstrates superiority over existing solutions based on neural networks. We show that the large margin of improvement is due to both the architecture of the model and the quality of the new training data set. This work opens up opportunities for developing new lightweight and accurate models for protein stability assessment. PROSTATA is available at https://github.com/AIRI-Institute/PROSTATA.

bioinformatics↗

bioRxiv2022

Cell type-specific interpretation of noncoding variants using deep learning-based methods

Interpretation of non-coding genomic variants is one of the most important challenges in human genetics. Machine learning methods have emerged recently as a powerful tool to solve this problem. State-of-the-art approaches allow prediction of transcriptional and epigenetic effects caused by non-coding mutations. However, these approaches require specific experimental data for training and can not generalize across cell types where required features were not experimentally measured. We show here that available epigenetic characteristics of human cell types are extremely sparse, limiting those approaches that rely on specific epigenetic input. We propose a new neural network architecture, DeepCT, which can learn complex interconnections of epigenetic features and infer unmeasured data from any available input. Furthermore, we show that DeepCT can learn cell type-specific properties, build biologically meaningful vector representations of cell types and utilize these representations to generate cell type-specific predictions of the effects of non-coding variations in the human genome.

genetics↗