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Short-tandem repeats (STRs) are the type of genetic markers extensively utilized in biomedical and forensic applications. Due to sequencing noise in nanopore sequencing, accurate analysis methods are lacking. We developed NASTRA, an innovative tool for Nanopore Autosomal Short Tandem Repeat Analysis, which overcomes traditional database-based methods' limitations and provides a precise germline analysis of STR genetic markers without the need for allele sequence reference. Demonstrating high accuracy in cell line authentication testing and paternity testing, NASTRA significantly surpasses existing methods in both speed and accuracy. This advancement makes it a promising solution for rapid cell line authentication and kinship testing, highlighting the potential of nanopore sequencing for in-field applications. [ABSTRACT FROM AUTHOR]

Deriving protein function from protein sequences poses a significant challenge due to the intricate relationship between sequence and function. Deep learning has made remarkable strides in predicting sequence-function relationships. However, models tailored for specific tasks or protein types encounter difficulties when using transfer learning across domains. This is attributed to the fact that protein function relies heavily on structural characteristics rather than mere sequence information. Consequently, there is a pressing need for a model capable of capturing shared features among diverse sequence-function mapping tasks to address the generalization issue. In this study, we explore the potential of Model-Agnostic Meta-Learning combined with a protein language model called Evolutionary Scale Modeling to tackle this challenge. Our approach involves training the architecture on five out-domain deep mutational scanning (DMS) datasets and evaluating its performance across four key dimensions. Our findings demonstrate that the proposed architecture exhibits satisfactory performance in terms of generalization and employs an effective few-shot learning strategy. To explain further, Compared to the best results, the Pearson's correlation coefficient (PCC) in the final stage increased by ~0.31%. Furthermore, we leverage the trained architecture to predict binding affinity scores of the DMS dataset of SARS-CoV-2 using transfer learning. Notably, training on a subset of the Ube4b dataset with 500 samples resulted in a notable improvement of 0.11 in the PCC. These results underscore the potential of our conceptual architecture as a promising methodology for multi-task protein function prediction., (© The Author(s) 2025. Published by Oxford University Press.)