Detalhe da pesquisa
1.
Bayesian LASSO for population stratification correction in rare haplotype association studies.
Stat Appl Genet Mol Biol
; 23(1)2024 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38235525
2.
Population stratification correction using Bayesian shrinkage priors for genetic association studies.
Ann Hum Genet
; 87(6): 302-315, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37771252
3.
Are dropout imputation methods for scRNA-seq effective for scHi-C data?
Brief Bioinform
; 22(4)2021 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33201180
4.
HiCImpute: A Bayesian hierarchical model for identifying structural zeros and enhancing single cell Hi-C data.
PLoS Comput Biol
; 18(6): e1010129, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35696429
5.
Sparse estimation in semiparametric finite mixture of varying coefficient regression models.
Biometrics
; 79(4): 3445-3457, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37066855
6.
Detecting X-linked common and rare variant effects in family-based sequencing studies.
Genet Epidemiol
; 45(1): 36-45, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32864779
7.
Evaluation and comparison of methods for recapitulation of 3D spatial chromatin structures.
Brief Bioinform
; 20(4): 1205-1214, 2019 07 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29091999
8.
Three-dimensional analysis reveals altered chromatin interaction by enhancer inhibitors harbors TCF7L2-regulated cancer gene signature.
J Cell Biochem
; 120(3): 3056-3070, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30548288
9.
Agonist and antagonist switch DNA motifs recognized by human androgen receptor in prostate cancer.
EMBO J
; 34(4): 502-16, 2015 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25535248
10.
A Family-Based Rare Haplotype Association Method for Quantitative Traits.
Hum Hered
; 83(4): 175-195, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30799419
11.
Are rare variants really independent?
Genet Epidemiol
; 41(4): 363-371, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28300291
12.
Statistical methods for detecting differentially methylated regions based on MethylCap-seq data.
Brief Bioinform
; 17(6): 926-937, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26454095
13.
Indirect effect inference and application to GAW20 data.
BMC Genet
; 19(Suppl 1): 67, 2018 09 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30255768
14.
Detecting associations of rare variants with common diseases: collapsing or haplotyping?
Brief Bioinform
; 16(5): 759-68, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25596401
15.
Logistic Bayesian LASSO for genetic association analysis of data from complex sampling designs.
J Hum Genet
; 62(9): 819-829, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28424482
16.
A random effect model for reconstruction of spatial chromatin structure.
Biometrics
; 73(1): 52-62, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27214023
17.
Detecting rare and common haplotype-environment interaction under uncertainty of gene-environment independence assumption.
Biometrics
; 73(1): 344-355, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27478935
18.
Impact of data resolution on three-dimensional structure inference methods.
BMC Bioinformatics
; 17: 70, 2016 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26852142
19.
GrammR: graphical representation and modeling of count data with application in metagenomics.
Bioinformatics
; 31(10): 1648-54, 2015 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25609792
20.
Block-based association tests for rare variants using Kullback-Leibler divergence.
J Hum Genet
; 61(11): 965-975, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27412875