CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing. Read more about CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing.
A Powerful Test for SNP Effects on Multivariate Binary Outcomes using Kernel Machine Regression. Read more about A Powerful Test for SNP Effects on Multivariate Binary Outcomes using Kernel Machine Regression.
POINT: Protein Structure Guided Local Test (R) Read more about POINT: Protein Structure Guided Local Test (R)
SparkScore: Leveraging Apache Spark for Distributed Genomic Inference. Read more about SparkScore: Leveraging Apache Spark for Distributed Genomic Inference.
ASSESSING ROBUSTNESS OF CLASSIFICATION USING ANGULAR BREAKDOWN POINT. Read more about ASSESSING ROBUSTNESS OF CLASSIFICATION USING ANGULAR BREAKDOWN POINT.
Robust Multicategory Support Vector Machines using Difference Convex Algorithm. Read more about Robust Multicategory Support Vector Machines using Difference Convex Algorithm.
SAFE-clustering: Single-cell Aggregated (from Ensemble) clustering for single-cell RNA-seq data. Read more about SAFE-clustering: Single-cell Aggregated (from Ensemble) clustering for single-cell RNA-seq data.
Efficient Estimation for Semiparametric Structural Equation Models With Censored Data. Read more about Efficient Estimation for Semiparametric Structural Equation Models With Censored Data.
Allele-specific copy-number discovery from whole-genome and whole-exome sequencing. Read more about Allele-specific copy-number discovery from whole-genome and whole-exome sequencing.
Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny. Read more about Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny.
