Genomic Sequencing Services

Whole genome Sequencing (Illumina, PacBio)

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

RNA-Sequencing (Single cell or bulk)

Iso-Seq (Full-length isoform Sequencing) on Pacbio Sequel II
Single cell RNA Sequencing on 10x Genomics Chromium and Illumina Sequencing platforms

Single-cell Sequencing

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

Microbiome Sequencing

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

Optical Whole Genome Mapping

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

Micro array

Illumina iScan system
Infinium genotyping arrays for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research

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