The rapid spread of misinformation on social media highlights the need for robust, automated fact correction frameworks.However, existing works rely on supervised learning from manually annotated claim-evidence pairs, which are scarce and prone to biases, limiting their generalization across domains.Moreover, these methods overlook semantic faithfulness in their correction process.To address these challenges, we propose Mask-to-Correct (M 2 C), a training-free, inference-only Retrieval Augmented Generation (RAG) based framework that leverages diversity-aware masking to identify erroneous spans of claims and evaluate the faithfulness of corrections using retrieved evidence.However, the effectiveness of RAG heavily depends on the choice of retriever, which may vary across queries.To mitigate this, we further introduce M 2 C + , an ensemblebased framework that combines corrections across multiple rankers to reduce retrieval bias and improve robustness.Extensive experiments on the benchmark datasets demonstrate that our proposed frameworks consistently outperform all baselines, achieving up to 14% improvement in SARI scores, without using gold evidence.

Leveraging both labeled (input-output associations) and unlabeled data (wider contextual grounding) may provide complementary benefits in retrieval augmented generation (RAG). However, effectively combining evidence from these heterogeneous sources is challenging as the respective similarity scores are not inter-comparable. Additionally, aggregating beliefs from the outputs of multiple rankers can improve the effectiveness of RAG. Our proposed method first aggregates the top-documents from a number of IR models using a standard rank fusion technique for each source (labeled and unlabeled). Next, we standardize the retrieval score distributions within each source by applying z-score transformation before merging the top-retrieved documents from the two sources. We evaluate our approach on the fact verification task, demonstrating that it consistently improves over the best-performing individual ranker or source and also shows better out-of-domain generalization.

Extraction of methodology component names from scientific articles is a challenging task due to the diversified contexts around the occurrences of these entities, and the different levels of granularity and containment relationships exhibited by these entities. We hypothesize that standard sequence labeling approaches may not adequately model the dependence of methodology name mentions with their contexts, due to the problems of their large, fast evolving, and domain-specific vocabulary. As a solution, we propose a factored approach, where the mention-context dependencies are represented in a more fine-grained manner, thus allowing the model parameters to better adjust to the different characteristic patterns inherent within the data. In particular, we experiment with two variants of this factored approach - one that uses the per-entity category information derived from an ontology, and the other that makes use of the topology of the sentence embedding space to infer a category for each entity constituting that sentence. We demonstrate that both these factored variants of SciBERT outperform their non-factored counterpart, a state-of-the-art model for scientific concept extraction.

Development of new drugs is an expensive and time-consuming process. Due to the world-wide SARS-CoV-2 outbreak, it is essential that new drugs for SARS-CoV-2 are developed as soon as possible. Drug repurposing techniques can reduce the time span needed to develop new drugs by probing the list of existing FDA-approved drugs and their properties to reuse them for combating the new disease. We propose a novel architecture DeepGLSTM, which is a Graph Convolutional network and LSTM based method that predicts binding affinity values between the FDA-approved drugs and the viral proteins of SARS-CoV-2. Our proposed model has been trained on Davis, KIBA (Kinase Inhibitor Bioactivity), DTC (Drug Target Commons), Metz, ToxCast and STITCH datasets. We use our novel architecture to predict a Combined Score (calculated using Davis and KIBA score) of 2,304 FDA-approved drugs against 5 viral proteins. On the basis of the Combined Score, we prepare a list of the top-18 drugs with the highest binding affinity for 5 viral proteins present in SARS-CoV-2. Subsequently, this list may be used for the creation of new useful drugs.

Interest in the habits of influential individuals cuts across domains. As researchers, we are intrigued why few attain significant eminence in their fields, whereas many operate in obscurity. An empirical examination of this question has been made possible by the recent availability of large scale publication data. In this paper, we use information from the AMiner Paper Citation and Author Collaboration Networks to discern factors that relate to the impact of influential researchers across five domains in the computing discipline. We propose and apply a novel algorithm to identify influential vertices in co-authorship networks built from total corpora of 1,00,000+ papers and 72,000+ authors over a span of more than 50 years. The results from our study indicate that the impact of these influential researchers relate to a variety of factors. Surprisingly, we find evidence across the domains that higher impact is associated with lower levels of collaboration, and authority.