GENOMICS

Sequencing

Genomics Sequencing Services — Platform & Deliverables

A genomics service matrix covering amplicon sequencing, metagenomics, transcriptomics, whole-genome resequencing, de novo sequencing and single-cell sequencing: sequencing strategy and data volume are matched to your research goals, with raw data and standard analysis reports delivered, and multi-omics integration with metabolomics/proteomics available.

Service List

SERVICE LIST

Eukaryotic RNA-seq

Amplicon Sequencing

Metagenomics

Whole Genome Sequencing

Single-cell RNA-seq

Sequencing Workflow

SERVICE WORKFLOW

Sample Intake

QC · registration

Library & Sequencing

Library prep · run

Data QC

Filtering · assessment

Bioinformatics

Composition / function / differential

Delivery

Data + report + Q&A

Notes: analysis modules and example figures for each service are detailed on the respective service pages (amplicon, metagenomics, RNA-seq); sequencing strategy, data volume and library prep are determined by research goals.

FAQ

How long does a Sequencing project take?

From sample QC approval, standard timelines are 3-6 weeks (library prep, sequencing and bioinformatics included); large cohorts or deep custom analyses follow the confirmed study plan.

What if my samples fail QC?

Failed QC is reported immediately with reasons, and we discuss resampling or plan adjustments with you — sequencing never proceeds without qualification.

What bioinformatics is included? Can I add custom analyses?

Standard delivery covers QC, mapping/assembly, quantification, differential and functional enrichment analyses. Custom deep-dive and multi-omics integrative analyses are supported on request.

What samples do you need for Sequencing?

Total RNA ≥1 μg with RIN ≥7 (snap-frozen, dry ice); microbial and faecal samples ≥200 mg (sterile, −80 °C); whole blood for WGS ≥500 μL (EDTA only, never heparin). RNA integrity matters more than concentration. See Technical Resources → Sample Guide.