Service Workflow

Phase 1. Consultation & Proposal

Please feel free to contact us. We will propose the most suitable analytical methods based on your specific research goals.

Phase 2. Sample Preparation & Quality Control (QC)

We extract high-quality DNA and verify its suitability for library construction. We then prepare libraries optimized for NGS. Estimated Timeline: 1–2 weeks

• Extraction of High Molecular Weight (HMW) DNA

• Assessment of DNA quality and purity

• Library preparation

Phase 3. Sequencing Execution

Using the latest NGS platforms, we perform high-depth, high-precision sequencing. We combine long-read, short-read, and Hi-C data to ensure comprehensive genome coverage tailored to the species and objective. Estimated Timeline: 1–2 weeks

• Long-read sequencing (PacBio / Oxford Nanopore)

• Short-read sequencing (Illumina)

• Hi-C library construction and sequencing

Phase 4. Genome Assembly & Annotation

Utilizing cutting-edge algorithms and high-performance computing resources, we perform high-precision de novo genome assembly. This is followed by gene prediction and functional annotation to build a comprehensive genomic database. Estimated Timeline: 1–2 weeks

• De novo assembly

• Gap closing

• Gene prediction and functional annotation

Phase 5. Data Analysis & Reporting

We conduct detailed analysis of genomic features and gene functions to create custom reports tailored to your needs. Our bioinformaticians provide professional interpretation and strategic insights. Estimated Timeline: 1–2 weeks

• Comparative genomic analysis

• Functional enrichment analysis

• Custom report generation