Piwi-interacting RNAs (piRNAs) play a pivotal role in maintaining genome integrity by repression of transposable elements, gene stability, and association with various disease progressions.Cost-efficient computational methods for the identification of piRNA disease associations promote the efficacy of disease-specific drug development.In this regard, we developed a simple, robust, here and efficient deep learning method for identifying the piRNA disease associations known as piRDA.The proposed architecture extracts the most significant and abstract information from raw sequences represented in a simplicated piRNA disease pair without any involvement of features engineering.Two-step positive unlabeled learning and bootstrapping technique are utilized to abstain from the false-negative and biased predictions dealing with positive unlabeled data.
The performance of proposed method piRDA is evaluated using k-fold cross-validation.The piRDA is significantly improved in all the performance evaluation measures for the identification of piRNA disease associations in comparison to state-of-the-art method.Moreover, it is thus projected conclusively that ps5 price new jersey the proposed computational method could play a significant role as a supportive and practical tool for primitive disease mechanisms and pharmaceutical research such as in academia and drug design.Eventually, the proposed model can be accessed using publicly available and user-friendly web tool athttp://nsclbio.jbnu.
ac.kr/tools/piRDA/.