Existing survival analysis techniques heavily rely on strong modelling assumptions and are, therefore, prone to model misspecification errors. In this paper, we develop an inferential method based on ideas from conformal prediction, which can wrap around any survival prediction algorithm to produce calibrated, covariate-dependent lower predictive bounds on survival times. In the Type I right-censoring setting, when the censoring times are completely exogenous, the lower predictive bounds have guaranteed coverage in finite samples without any assumptions other than that of operating on independent and identically distributed data points. Under a more general conditionally independent censoring assumption, the bounds satisfy a doubly robust property which states the following: marginal coverage is approximately guaranteed if either the censoring mechanism or the conditional survival function is estimated well. Further, we demonstrate that the lower predictive bounds remain valid and informative for other types of censoring. The validity and efficiency of our procedure are demonstrated on synthetic data and real COVID-19 data from the UK Biobank. 



This is joint work with Emmanuel Candès and Lihua Lei.

9 Jun 2021
11am - 12pm
Where
Online via ZOOM (ID: 999 8882 7320, Passcode: hkust)
Speakers/Performers
Dr. Zhimei REN
Stanford University
Organizer(S)
Department of Mathematics
Contact/Enquiries
Payment Details
Audience
Alumni, Faculty and staff, PG students
Language(s)
English
Other Events
26 Apr 2024
Seminar, Lecture, Talk
IAS / School of Science Joint Lecture - Molecular Basis of Wnt Biogenesis, Secretion and Ligand Specific Signaling
Abstract Wnt signaling is essential to regulate embryonic development and adult tissue homeostasis. Aberrant Wnt signaling is associated with cancers. The ER-resident membrane-bound O-acyltransfera...
18 Apr 2024
Seminar, Lecture, Talk
IAS / School of Science Joint Lecture - Understanding the Roles of Transposable Elements in the Human Genome
Abstract Transposable elements (TEs) have expanded the binding repertoire of many transcription factors and, through this process, have been co-opted in different transcriptional networks. In this ...