This is a project that I work with my student and what we actually did, we looked at the TP53 mutated multiple myeloma. They have conferred a poor prognosis, poor survival. So we look at those patients first and identify the cohort who are doing the worst and have a poor survival. Then we extract the genes that actually interplay a role in those TP53-mutated multiple myelomas and their pathways, how they’ve been interconnected...
This is a project that I work with my student and what we actually did, we looked at the TP53 mutated multiple myeloma. They have conferred a poor prognosis, poor survival. So we look at those patients first and identify the cohort who are doing the worst and have a poor survival. Then we extract the genes that actually interplay a role in those TP53-mutated multiple myelomas and their pathways, how they’ve been interconnected. So we have gene expressions, we have a gene pathway. Then we use the machine learning model actually try to predict how they’re going to do over the period of years, so we use the CoxBoost analysis, LASSO analysis, and different types of machine learning algorithms, and try to predict whether the molecular profiling, and if you use the clinical profiling in that, is this a better predictor or not? And according to the scatter plot that we plotted on this machine learning model, we found that the best-fitted model is the CoxBoost model. So I think that incorporating machine learning into the genomic findings and the clinical behavior is the way to go in the future.
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