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
- For further information contact us here
