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Harman Singh

Publications and source records attributed to Harman Singh.

20 records · Page 2Linked to original sources

FaiRR: Faithful and Robust Deductive Reasoning over Natural Language

Transformers have been shown to be able to perform deductive reasoning on a logical rulebase containing rules and statements written in natural language. Recent works show that such models can also produce the reasoning steps (i.e., the proof graph) that emulate the model's logical reasoning process. Currently, these black-box models generate both the proof graph and intermediate inferences within the same model and thus may be unfaithful. In this work, we frame the deductive logical reasoning task by defining three modular components: rule selection, fact selection, and knowledge composition. The rule and fact selection steps select the candidate rule and facts to be used and then the knowledge composition combines them to generate new inferences. This ensures model faithfulness by assured causal relation from the proof step to the inference reasoning. To test our framework, we propose FaiRR (Faithful and Robust Reasoner) where the above three components are independently modeled by transformers. We observe that FaiRR is robust to novel language perturbations, and is faster at inference than previous works on existing reasoning datasets. Additionally, in contrast to black-box generative models, the errors made by FaiRR are more interpretable due to the modular approach.

cs.CL↗

Unlocking capacities of viral genomics for the COVID-19 pandemic response

More than any other infectious disease epidemic, the COVID-19 pandemic has been characterized by the generation of large volumes of viral genomic data at an incredible pace due to recent advances in high-throughput sequencing technologies, the rapid global spread of SARS-CoV-2, and its persistent threat to public health. However, distinguishing the most epidemiologically relevant information encoded in these vast amounts of data requires substantial effort across the research and public health communities. Studies of SARS-CoV-2 genomes have been critical in tracking the spread of variants and understanding its epidemic dynamics, and may prove crucial for controlling future epidemics and alleviating significant public health burdens. Together, genomic data and bioinformatics methods enable broad-scale investigations of the spread of SARS-CoV-2 at the local, national, and global scales and allow researchers the ability to efficiently track the emergence of novel variants, reconstruct epidemic dynamics, and provide important insights into drug and vaccine development and disease control. Here, we discuss the tremendous opportunities that genomics offers to unlock the effective use of SARS-CoV-2 genomic data for efficient public health surveillance and guiding timely responses to COVID-19.

q-bio.GN↗