Genomics support in Indonesia
GSN helps universities, research institutes, hospitals, and companies choose a suitable workflow, prepare samples, arrange shipment, and define the data or analysis they need.
How a project moves
Bioinformatics
Select a workflow and analysis level. Higher levels include the deliverables from the lower levels unless stated otherwise.
Human analysis can use hg19 or GRCh38. Higher levels include the outputs from lower levels.
Demultiplexed and adapter-trimmed FASTQ
Metrics in CSV format
MultiQC report in HTML
Research services
Search by method, sample, or research goal. Open a service page for its usual applications, input material, and available outputs.
DNA & Genome
Whole genome sequencing service with short-read and HiFi long-read pathways for variant discovery, comparative genomics, and de novo assembly.
DNA & Genome
Whole exome and targeted sequencing service for protein-coding regions, selected genes, and custom genomic targets.
RNA & Transcriptome
RNA sequencing (RNA-seq) service for coding or whole-transcriptome profiling, isoform discovery, and differential analysis.
RNA & Transcriptome
Single-cell RNA sequencing service to resolve cellular heterogeneity and connect expression patterns with tissue morphology.
Microbiome
Metagenomic sequencing service with shotgun metagenomics or full-length 16S rRNA profiling for community insight.
Oncology & Immunology
Research-use tumor profiling NGS service with focused, comprehensive, and liquid-biopsy approaches.
Oncology & Immunology
Immune profiling service with HLA typing, T-cell receptor sequencing, and single-cell analysis for immunology projects.
Sanger & Oligo
Sanger DNA sequencing service for sequence confirmation, plasmids, PCR products, and custom primers by tube or plate.
RNA & Transcriptome
miRNA and small RNA sequencing service for short regulatory transcripts, biomarkers, and expression research.
Epigenomics
DNA methylation sequencing service with genome-wide or long-read approaches for epigenomic research.
DNA & Genome
Sequencing-only service for compatible customer-prepared libraries using high-capacity short-read or long-read sequencing.
Data & Bioinformatics
NGS bioinformatics analysis services that turn raw reads into interpretable outputs with project-matched pipelines.
Sample preparation
These are practical planning values adapted to the available service workflows. Always wait for project-specific confirmation before shipment.
Typical planning values
Technology guide
The required output, sample quality, genome complexity, and study design determine whether short reads, long reads, or Sanger sequencing are suitable.
Well suited to variant discovery, gene-expression quantification, microbiome profiling, and projects needing scalable data output.
Useful for de novo assembly, complex regions, isoforms, phasing, structural variation, and native methylation analysis.
A direct route for PCR products, plasmids, clone checks, and targeted confirmation using one or more sequencing primers.
Project workflow
Choose a stage to see what we review and what information is needed next.
Selected stage
We translate your research objective into a practical sequencing plan, then confirm sample count, organism, output, analysis scope, budget assumptions, and timeline.
Scientific objective and comparison groups
Organism or clinical context
Sample count and available material
Required output and analysis
Working with GSN
GSN coordinates project design, sample preparation, shipment, quotation, and communication for teams in Indonesia.
Discuss organism, design, coverage, output, controls, and analysis before committing budget or sending samples.
Review sample readiness, documentation, packaging, and the correct shipment pathway before dispatch.
Receive an official local quotation and invoice, including tax-document support where applicable.
Keep sample IDs, requirements, data scope, contacts, and delivery expectations traceable from enquiry to result.
GSN coordinates consultation, local administration, and project communication. The performing laboratory, test configuration, applicable quality framework, sample acceptance criteria, and turnaround time are stated in the official quotation.
Common questions
For a project-specific answer, send a short brief with the sample type, sample count, objective, and timeline.
Email scientific supportNo. Start with the research objective, organism, sample type, sample count, and expected result. Platform, read type, and output can then be matched to the question.
GSN coordinates research workflows for whole genome and exome sequencing, RNA-seq, single-cell RNA sequencing, metagenomics and 16S rRNA, Sanger sequencing, long-read sequencing, methylation sequencing, tumor and immune profiling, plus NGS bioinformatics analysis. The final configuration is matched to the sample, study design, and intended output.
Cost depends on the sequencing method, sample count, genome size, target output or coverage, library-preparation requirements, and bioinformatics scope. Send a project brief to receive a clearly defined configuration and quotation.
Yes. Include the proposal deadline, estimated sample count, preferred scope, and whether bioinformatics is required. Assumptions will be stated clearly in the quotation.
Extraction and QC coordination can be discussed for different sample types. Available measurements may include fluorometric quantification, electrophoresis, and fragment-integrity assessment, subject to the agreed workflow.
The issue and available options are reviewed before continuing. Depending on the workflow, options may include re-extraction, replacement, an adapted protocol, or proceeding with an acknowledged risk.
Yes. Tube and 96-well submissions can be prepared for Sanger sequencing, while custom primer or oligo orders can specify sequence, scale, purification, modification, and format.
The quotation defines deliverables. These may range from raw FASTQ files and QC reports to alignment files, variants, count matrices, assemblies, taxonomy tables, or structured analysis reports.
Project enquiry
You do not need to know the platform or output yet. The objective, sample type, sample count, organism, and timeline are enough to begin.
