Xin Li 0061

dblp:09/1365-61 · DBLP profile ↗
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3ranked-venue papers
3as first author
2since 2021 · last 2024
0000-0002-7536-6782ORCID · conflict

Domains — the database's venue-derived domains; a paper can count in several

Theory of computation · 2 · 2 first-author · 2 since 2021Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author
YearPublicationVenuePosition
2024 Low-rank matrix estimation via nonconvex optimization methods in multi-response errors-in-variables regression
Xin Li 0061, Dongya Wu
J. Glob. Optim.1
2023 Sparse estimation via lower-order penalty optimization methods in high-dimensional linear regression
Xin Li 0061, Chong Li 0002, Xiaoqi Yang 0001, Tianzi Jiang
J. Glob. Optim.1
2019 Reliable heritability estimation using sparse regularization in ultrahigh dimensional genome-wide association studies
abstract
BACKGROUND: Data from genome-wide association studies (GWASs) have been used to estimate the heritability of human complex traits in recent years. Existing methods are based on the linear mixed model, with the assumption that the genetic effects are random variables, which is opposite to the fixed effect assumption embedded in the framework of quantitative genetics theory. Moreover, heritability estimators provided by existing methods may have large standard errors, which calls for the development of reliable and accurate methods to estimate heritability. RESULTS: In this paper, we first investigate the influences of the fixed and random effect assumption on heritability estimation, and prove that these two assumptions are equivalent under mild conditions in the theoretical aspect. Second, we propose a two-stage strategy by first performing sparse regularization via cross-validated elastic net, and then applying variance estimation methods to construct reliable heritability estimations. Results on both simulated data and real data show that our strategy achieves a considerable reduction in the standard error while reserving the accuracy. CONCLUSIONS: The proposed strategy allows for a reliable and accurate heritability estimation using GWAS data. It shows the promising future that reliable estimations can still be obtained with even a relatively restricted sample size, and should be especially useful for large-scale heritability analyses in the genomics era.
Xin Li 0061, Dongya Wu, Yue Cui 0005, Bing Liu 0008, Henrik Walter, Gunter Schümann, Chong Li 0002, Tianzi Jiang
BMC Bioinform.1