DSO National Laboratories Singapore
Abstract:Colorectal cancer is the most common cancer in Singapore and the third most common cancer worldwide. Blood in a person's stool is a symptom of this disease, and it is usually detected by the faecal occult blood test (FOBT). However, the FOBT presents several limitations - the collection process for the stool samples is tedious and unpleasant, the waiting period for results is about 2 weeks and costs are involved. In this research, we propose a simple-to-use, fast and cost-free alternative - a stool recognition neural network that determines if there is blood in one's stool (which indicates a possible risk of colorectal cancer) from an image of it. As this is a new classification task, there was limited data available, hindering classifier performance. Hence, various Generative Adversarial Networks (GANs) (DiffAugment StyleGAN2, DCGAN, Conditional GAN) were trained to generate images of high fidelity to supplement the dataset. Subsequently, images generated by the GAN with the most realistic images (DiffAugment StyleGAN2) were concatenated to the classifier's training batch on-the-fly, improving accuracy to 94%. This model was then deployed to a mobile app - Poolice, where users can take a photo of their stool and obtain instantaneous results if there is blood in their stool, prompting those who do to seek medical advice. As "early detection saves lives", we hope our app built on our stool recognition neural network can help people detect colorectal cancer earlier, so they can seek treatment and have higher chances of survival.
Abstract:More infectious virus variants can arise from rapid mutations in their proteins, creating new infection waves. These variants can evade one's immune system and infect vaccinated individuals, lowering vaccine efficacy. Hence, to improve vaccine design, this project proposes Optimus PPIme - a deep learning approach to predict future, more infectious variants from an existing virus (exemplified by SARS-CoV-2). The approach comprises an algorithm which acts as a "virus" attacking a host cell. To increase infectivity, the "virus" mutates to bind better to the host's receptor. 2 algorithms were attempted - greedy search and beam search. The strength of this variant-host binding was then assessed by a transformer network we developed, with a high accuracy of 90%. With both components, beam search eventually proposed more infectious variants. Therefore, this approach can potentially enable researchers to develop vaccines that provide protection against future infectious variants before they emerge, pre-empting outbreaks and saving lives.