scholarly article | Q13442814 |
P819 | ADS bibcode | 2015PLoSO..1035918W |
P356 | DOI | 10.1371/JOURNAL.PONE.0135918 |
P932 | PMC publication ID | 4547758 |
P698 | PubMed publication ID | 26302001 |
P5875 | ResearchGate publication ID | 281519012 |
P50 | author | Chuhsing Kate Hsiao | Q56928951 |
P2093 | author name string | Charlotte Wang | |
Wen-Hsin Kao | |||
P2860 | cites work | SKM-SNP: SNP markers detection method. | Q51774451 |
Error Detecting and Error Correcting Codes | Q55871133 | ||
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression | Q21092443 | ||
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
An approach for clustering gene expression data with error information | Q25257101 | ||
The ENCODE (ENCyclopedia Of DNA Elements) Project | Q29547219 | ||
Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression | Q30428383 | ||
Cluster analysis of genetic and epidemiological data in molecular epidemiology | Q31159953 | ||
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci. | Q33855434 | ||
Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies. | Q33904871 | ||
Nonparametric tests of association of multiple genes with human disease | Q33942281 | ||
Using an uncertainty-coding matrix in Bayesian regression models for haplotype-specific risk detection in family association studies | Q33971149 | ||
Gene-based tests of association | Q33987507 | ||
A Framework for Feature Selection in Clustering | Q34095100 | ||
Powerful SNP-set analysis for case-control genome-wide association studies | Q34544433 | ||
Gene-based testing of interactions in association studies of quantitative traits | Q34611220 | ||
Assessing methods for assigning SNPs to genes in gene-based tests of association using common variants | Q34760371 | ||
Generalized genomic distance-based regression methodology for multilocus association analysis | Q35221489 | ||
Sequence kernel association tests for the combined effect of rare and common variants | Q36909285 | ||
U-statistics-based tests for multiple genes in genetic association studies | Q36952464 | ||
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease | Q37211205 | ||
Gene-trait similarity regression for multimarker-based association analysis. | Q37356869 | ||
Statistical analysis strategies for association studies involving rare variants | Q37799723 | ||
Rare variant association analysis methods for complex traits | Q37806780 | ||
Analysing biological pathways in genome-wide association studies | Q37810464 | ||
Determining the number of clusters using the weighted gap statistic | Q48405971 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Hamming distance | Q272172 |
P304 | page(s) | e0135918 | |
P577 | publication date | 2015-08-24 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Using Hamming Distance as Information for SNP-Sets Clustering and Testing in Disease Association Studies | |
P478 | volume | 10 |
Q36373005 | A latent genetic subtype of major depression identified by whole-exome genotyping data in a Mexican-American cohort |
Q38632950 | AveDissR: An R function for assessing genetic distinctness and genetic redundancy |
Q51556717 | Re-examining Dis/Similarity-Based Tests for Rare-Variant Association with Case-Control Samples. |
Q61810720 | SNP variable selection by generalized graph domination |
Q33734235 | Structure-Leveraged Methods in Breast Cancer Risk Prediction |
Q47380958 | Unlocking the diversity of genebanks: whole-genome marker analysis of Swiss bread wheat and spelt. |
Q55074868 | Utility of Genetic Testing in Addition to Mammography for Determining Risk of Breast Cancer Depends on Patient Age. |
Search more.