SEQUENCING SERVICES IN INDONESIA
Explore whole genome sequencing, whole exome sequencing, RNA-seq, single-cell, metagenomics, full-length 16S rRNA, Sanger sequencing, long-read workflows, and bioinformatics through one coordinated project pathway.
COMPLETE RESEARCH PORTFOLIO
Each page explains applications, starting material, possible deliverables, available pathways, and the decisions needed before quotation.
DNA & Genome
This whole genome sequencing service supports short-read and HiFi long-read workflows for variant discovery, comparative genomics, and de novo assembly.
DNA & Genome
This whole exome sequencing service supports efficient investigation of protein-coding regions, selected genes, and custom genomic targets.
RNA & Transcriptome
This RNA sequencing (RNA-seq) service supports coding and whole-transcriptome profiling, gene-expression analysis, isoform discovery, and differential analysis.
RNA & Transcriptome
This single-cell RNA sequencing service resolves cellular heterogeneity and connects gene-expression patterns with cell populations or tissue morphology.
Microbiome
This metagenomic sequencing service offers shotgun metagenomics and full-length 16S rRNA sequencing for taxonomic and functional community profiling.
Oncology & Immunology
This research-use tumor profiling NGS service supports focused or comprehensive molecular profiling and liquid-biopsy research workflows.
Oncology & Immunology
This immune profiling service combines HLA typing, T-cell receptor sequencing, and single-cell immune profiling for immunology research.
Sanger & Oligo
This Sanger DNA sequencing service supports tube or plate submissions for sequence confirmation, plasmids, PCR products, and custom primers.
RNA & Transcriptome
This miRNA and small RNA sequencing service profiles short regulatory transcripts for biomarker, expression, and functional research.
Epigenomics
This DNA methylation sequencing service supports genome-wide and long-read approaches for studying methylation patterns and epigenomic change.
DNA & Genome
This sequencing-only service provides high-capacity short-read or long-read sequencing for compatible, customer-prepared libraries.
Data & Bioinformatics
These NGS bioinformatics analysis services turn raw sequencing reads into interpretable outputs using project-matched pipelines and clear deliverables.
SEARCH BY RESEARCH CONTEXT
These groups cover common ways researchers look for sequencing support—by organism, material, application, technology, and desired analysis.
Plan human, bacterial, fungal, plant, animal, fish, insect, or other genome projects using short-read WGS, PacBio HiFi long-read sequencing, exome capture, targeted sequencing, de novo assembly, or reference-based analysis.
Explore genome sequencing →Choose bulk RNA sequencing, coding or whole-transcriptome analysis, small RNA and miRNA sequencing, single-cell RNA sequencing, or spatial transcriptomics according to the biological question and sample condition.
Explore RNA sequencing →Compare shotgun metagenomic sequencing with full-length 16S rRNA sequencing for taxonomic profiling, microbial diversity, functional analysis, and environmental or host-associated microbiome studies.
Explore microbiome sequencing →Define whether the project should deliver raw FASTQ, quality-controlled reads, mapping, variant calls, expression matrices, genome assembly, taxonomy, statistical analysis, figures, or a structured report.
Explore bioinformatics services →SEQUENCING SERVICE FAQ
Use these answers for initial planning. The final method, sample acceptance, output, turnaround, and price are confirmed for each project.
Build a project briefGSN coordinates research workflows for whole genome and exome sequencing, RNA-seq, single-cell RNA sequencing, small RNA and miRNA, metagenomics and full-length 16S rRNA, Sanger sequencing, DNA methylation, tumor and immune profiling, sequencing-only libraries, and NGS bioinformatics analysis.
Pricing depends on sample number, organism and genome size, library preparation, platform, read type, target output or coverage, and the required bioinformatics level. A project brief is reviewed before an official quotation is issued.
Short reads are commonly used for scalable quantification and small-variant analysis. HiFi long reads support de novo assembly, phasing, isoforms, complex regions, and structural variants. Sanger sequencing is a focused option for PCR products, plasmids, and targeted sequence confirmation.
Yes. The project is configured according to organism, genome size, ploidy, reference availability, sample quality, research objective, and the intended analysis. Eligibility and final specifications are confirmed during scientific review.
Yes. Existing sequencing data can be reviewed for QC, mapping, variant analysis, expression analysis, assembly, microbiome profiling, statistics, and visualization when the files, metadata, study design, and reference information are suitable.
Provide the research objective, organism, sample type, number of samples, available QC measurements, required output, analysis scope, and preferred timeline. Missing technical details can be resolved during project consultation.
READY TO PLAN THE PROJECT?
