We provide support in the design and analysis of your NGS experiments.

Core analysts have extensive experience in  managing and analyzing sequencing data, including:

• single-cell and single-nuclei RNA-seq
• RNA-seq (quantification and de novo transcriptome analysis)
• ChIP-seq and ATAC-seq
• whole genome and exome sequencing (quality control, mapping, re-alignment, variant calls, prioritization)
• small RNA-seq (i.e. miRNA analysis)
• bisulfite sequencing and DNA methylation arrays
• genome assembly (reference guided and de novo)
• custom NGS analyses