- Variant discovery
- De novo assembly
- Comparative genomics
- Population studies
DNA & GENOME · SERVICE 01
Whole Genome Sequencing (WGS) for research teams in Indonesia.
Short-read and HiFi long-read pathways for variant discovery, comparative genomics, and de novo assembly.
Layanan whole genome sequencing (WGS) untuk tim riset di Indonesia, dengan pilihan short-read atau HiFi long-read serta dukungan analisis varian dan perakitan genom.
The right pathway depends on organism, reference availability, genome size, ploidy, structural-variant needs, and DNA integrity.
Sample acceptance, technology, output, analysis scope, turnaround, and price are confirmed after scientific review and in the official quotation.
AVAILABLE PATHWAYS
Shape the workflow around the biological question.
These pathways are a project-planning guide. The final configuration is selected after the organism, material, study design, and intended deliverables are reviewed.
Short-read WGS
Discuss suitability, sample requirements, output, and analysis options with scientific support.
HiFi long-read WGS
Discuss suitability, sample requirements, output, and analysis options with scientific support.
Reference-based analysis
Discuss suitability, sample requirements, output, and analysis options with scientific support.
De novo assembly
Discuss suitability, sample requirements, output, and analysis options with scientific support.
BEFORE REQUESTING A QUOTATION
Three details make the first discussion more useful.
- 01Define the research question
State the biological decision, hypothesis, or comparison the data should support.
- 02Describe the material
Share sample type, organism, quantity, quality measurements, and number of samples.
- 03Choose the handover level
Clarify whether you need raw data, processed files, advanced analysis, or a structured report.
READY TO PLAN THE PROJECT?