Genomic Sequencing Services

  • PacBio HiFi long read sequencing on Sequel II (for de novo genome assembly, Variant detection or structural variant detection)
  • PCR free short read sequencing on Illumina NovaSeq 6000
  • Iso-Seq (Full-length isoform Sequencing) on Pacbio Sequel II
  • Single cell RNA Sequencing on 10x Genomics Chromium and Illumina Sequencing platforms
  • Single cell Immuno-Profiling: Analyze the immune repertoires of individual B and T cells
  • Single cell gene expression: Provide single-cell transcriptome 3’ gene expression profile
  • Single cell ATAC-Seq: Analyze chromatin accessibility
  • 10x Genomics Chromium and Illumina Sequencing flatforms
  • Sequencing either the V1–V3 or V4 region of the 16S rRNA gene on Illumina sequencing platform
  • Sequencing the full 16S rRNA gene on Illumina sequencing
  • Sequencing the 16S-ITS-23S region on PacBio Sequel or Sequel II (strain identification)
  • Shotgun metagenomic sequencing
  • Identification of structural variation by ultra-high molecular weight DNA extraction, labeling and imaging on Bionano Saphyr system
  • De novo assembly
  • Hybrid scaffolding with NGS data for genome completion
  • Long range information at high coverage for cancer genome research
  • Illumina iScan system
  • Infinium genotyping arrays for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research