Services Available

QC of FASTQ files using FASTQC 
Alignment of sequencing reads to the appropriate reference genome using BWA  
Variant calling using GATK 
Differential expression pipelines using STAR, RUVseq, and edgeR 
Single-cell pipelines using Seurat  
Differential methylation analysis  
Polygenic risk score and genetic correlation analysis using PRsice  
Tissue-specific variant annotation 
Advanced network analysis  
Transcriptome imputation  
Transcriptome-based drug repositioning  
Machine learning