Analysis of gait pattern related to high cerebral small vessel disease burden using quantitative gait data from wearable sensors.

PGG.SV: a whole-genome-sequencing-based structural variant resource and data analysis platform.

Forecasting and Evaluating Multiple Interventions for COVID-19 Worldwide.

PreMedKB: an integrated precision medicine knowledgebase for interpreting relationships between diseases, genes, variants and drugs.

SeleDiff: A fast and scalable tool for estimating and testing selection differences between populations.

knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable.

Random Bits Regression: a Strong General Predictor for Big Data.

Efficient test for nonlinear dependence of two continuous variables.

Evaluation of copy number variation detection for a SNP array platform.

Detecting Genetic Association of Common Human Facial Morphological Variation Using High Density 3D Image Registration.

Gene co-expression network and functional module analysis of ovarian cancer.

Integrated analysis of mutations, miRNA and mRNA expression in glioblastoma.

Novel statistical framework to identify differentially expressed genes allowing transcriptomic background differences.

HaploBlockFinder: Haplotype Block Analyses.