Abstract:Instruction-tuned large language models, such as T0, have demonstrated remarkable capabilities in following instructions across various domains. However, their proficiency remains notably deficient in many low-resource languages. To address this challenge, we introduce FarsInstruct: a comprehensive instruction dataset designed to enhance the instruction-following ability of large language models specifically for the Persian language, a significant yet underrepresented language globally. FarsInstruct encompasses a wide range of task types and datasets, each containing a mix of straightforward to complex manual written instructions, as well as translations from Public Pool of Prompts, ensuring a rich linguistic and cultural representation. Furthermore, we introduce Co-CoLA, a framework designed to enhance the multi-task adaptability of LoRA-tuned models. Through extensive experimental analyses, our study showcases the effectiveness of FarsInstruct dataset coupled with training by Co-CoLA framework, in improving the performance of large language models within the Persian context. As of the current writing, FarsInstruct comprises more than 200 templates across 21 distinct datasets, and we intend to update it consistently, thus augmenting its applicability.
Abstract:This study analyzes crop yield prediction in India from 1997 to 2020, focusing on various crops and key environmental factors. It aims to predict agricultural yields by utilizing advanced machine learning techniques like Linear Regression, Decision Tree, KNN, Na\"ive Bayes, K-Mean Clustering, and Random Forest. The models, particularly Na\"ive Bayes and Random Forest, demonstrate high effectiveness, as shown through data visualizations. The research concludes that integrating these analytical methods significantly enhances the accuracy and reliability of crop yield predictions, offering vital contributions to agricultural data science.
Abstract:Understanding cell identity is an important task in many biomedical areas. Expression patterns of specific marker genes have been used to characterize some limited cell types, but exclusive markers are not available for many cell types. A second approach is to use machine learning to discriminate cell types based on the whole gene expression profiles (GEPs). The accuracies of simple classification algorithms such as linear discriminators or support vector machines are limited due to the complexity of biological systems. We used deep neural networks to analyze 1040 GEPs from 16 different human tissues and cell types. After comparing different architectures, we identified a specific structure of deep autoencoders that can encode a GEP into a vector of 30 numeric values, which we call the cell identity code (CIC). The original GEP can be reproduced from the CIC with an accuracy comparable to technical replicates of the same experiment. Although we use an unsupervised approach to train the autoencoder, we show different values of the CIC are connected to different biological aspects of the cell, such as different pathways or biological processes. This network can use CIC to reproduce the GEP of the cell types it has never seen during the training. It also can resist some noise in the measurement of the GEP. Furthermore, we introduce classifier autoencoder, an architecture that can accurately identify cell type based on the GEP or the CIC.