Next Generation Sequencing

The Genomics Shared Resource provides NGS library preparation, sequence enrichment and sequencing services for use on the Illumina NovaSeq, Illumina NextSeq, and Illumina MiSeq sequencing systems. We also validate NGS findings using Agena, Illumina, SYBR green PCR and Sanger sequencing platforms.

 

  • Whole Genome Sequencing
  • Whole Exome Sequencing
    • Agilent SureSelect
    • Illumina Nextera DNA Exome
  • DNA Methylation
    • Whole Genome Bisulfite Sequencing (WGBS)
    • Reduced-Representation Bisulfite Sequencing (RRBS)
    • MethylCapture-seq
  • RNA Sequencing
    • mRNA Seq
    • Whole transcriptome
    • RNA-Exome (FFPE RNA)
    • Ultra-low Input
    • Small RNA Seq (miRNA-seq)
  • Metagenomics
    • 16S Sequencing
    • Whole Genome -Shotgun Metagenomics Sequencing
  • Targeted-Sequencing
    • AmpliSeq for Illumina
    • ArcherDx
    • Custom amplicon
    • CRISPR screening
    • shRNA screening
  • TCR-Seq
  • ChIP-Seq