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does not require auxiliary matching information for
the alignment. In particular, our method can align
longitudinal data across heterogeneous subjects in a
common latent space to capture the dynamics of
shared patterns while utilizing temporal dependency
within subjects. Our numerical studies on both simulation settings and neuronal activity data indicate that
the proposed data integration approach improves prediction accuracy compared to existing machine learning methods.
Joint work with Yubai Yuan, Babak Shahbaba, Robert Fortin, Keiland Cooper and Qing Nie.
Estimating Heritability of Time-to-Event Traits
Using Censored Multiple Variance Component
Model
Jin Zhou
University of California, Los Angeles
Abstract: Genome-wide association studies (GWASs)
have spotlighted genetic variants linked to the onset
age for diseases such as Type 2 diabetes, Alzheimer's,
and heart disease. Central to GWASs is heritability,
which represents the proportion of phenotypic variation attributable to genetic variation. Historical approaches rooted in animal breeding are inadequate for
modern human genomic data. Alternatively, heritability relies on binary disease-status traits that fail to
capture the temporal aspect of disease development.
In this context, our research presents the censored multiple variance component model (CMVC)
based on an accelerated failure time model with
syntenic variables. Designed for individual-level genotype data, it's scalable for biobank data and handles
time-to-event data with random right-censoring. Simulations affirm its unbiased nature for right-censored
outcomes. We offer heritability assessments for various diseases, explore per-allele effect sizes across
genomic segments, and apply our methods to UK
Biobank.
Conclusively, our study introduces an advanced
method tailored for human genomic data, shedding
profound insights into the genetic determinants of
disease onset and progression.
Invited Session IS073: Statistical Interdisciplinary
Studies II
A New Statistic That Integrates Statistical Significance and Clinical Significance for Assessing the
Progression of Pulmonary Nodules
Jing Zhou
Renmin University of China
Abstract: Lung cancer remains one of the most prevalent malignant tumors worldwide. Nearly all lung
cancers evolve from pulmonary nodules, which are
the lesions that manifest as distinct \"spots\" within the
lung areas. For most patients with diagnosed pulmonary nodules, achieving a benign/malignant diagnosis
only based on baseline CT scans is particularly challenging. Therefore, adopting regular follow-up treatment becomes one of the crucial strategies in clinical
practice. In this study, we develop a novel statistic that
would be able to quantify the changes in nodules observed between baseline and follow-up CT scans for
one specific patient. Compared with previous studies,
we have three significant contributions. Firstly, the
proposed statisitc relies solely on 2D CT images for
calculation, circumvents the cumbersome process
required by traditional volumetric methods that necessitate precise delineation of the nodule’s 3D shape.
Additionally, we provided the empirical distribution
of this metric, enabling hypothesis testing for change
detection. Secondly, we proposed a novel technique
for generating invariant nodule samples based on
Gaussian random perturbation, overcoming the limitations of existing studies that could only simulate invariant nodules based on phantom, and breaking
through the bottleneck in mass-producing invariant
nodule samples. Lastly, to make this method more
aligned with clinical practice, we innovatively introduced the concept of clinical significance. This ensures that the assessment of nodule progression not
only considers statistical significance but also incorporates the clinical experience of physicians, making
the test statistic proposed in this paper more valuable
for clinical application.
Joint work with Hang Yu, Hansheng Wang, Ying Ji.
Correlation Trilogy of UWF-Based Myopia Predic-