ARUNA Science and Technology

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LEADING EMPOWERMENT IN GENOMICS RESEARCH

Innovative Approaches to Genomic Discovery

Accelerate your research with advanced DNA & RNA sequencing services and customized multi-omic solutions tailored for global life sciences.

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Expert Consultation

Genomics Specialist

Global
Genomics Provider

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Our Solutions

Providing the best solutions
for your research

DNA Sequencing
RNA Sequencing
Customized Solutions
Antibodies & Reagents
DNA SEQUENCING

High-Throughput Genomic Decoding

Unlock complete genetic architectures with our comprehensive suite of Next-Generation Sequencing (NGS) and long-read technologies. We deliver unparalleled coverage and accuracy for human, plant, animal, and microbial genomes.

  • Whole Genome Re-sequencing
  • De Novo Sequencing
  • Whole Genome Bisulfite Sequencing
  • ChIP-Seq
  • Whole Genome Sequencing
  • Long-read Human Whole Genome Resequencing
  • Whole Exome Sequencing
  • 16S/18S/ITS Sequencing
  • Metagenomic Sequencing
Explore DNA Services Explore DNA Services
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Q30 GUARANTEE
Delivering high-fidelity multi-omic datasets globally.
UNCOMPROMISING QUALITY

Industry-Leading Standards in
Genomic Data Accuracy

We utilize state-of-the-art Next-Generation Sequencing (NGS) platforms alongside rigorous quality control pipelines to deliver publication-ready data for global researchers.

Base Calling Accuracy ( ≥ Q30 Quality Scores)
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Mapping & Alignment Rate (Reference Genome Match)
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On-Time Data Delivery & Technical Support
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  • ISO-compliant laboratories and strictly monitored pipelines
  • Comprehensive bioinformatics reports and raw data delivery
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WHY PARTNER WITH US

High-Throughput Platforms for
Accelerated Discovery

Our massive parallel sequencing infrastructure drastically cuts down turnaround times, allowing you to scale up projects from small pilot cohorts to large-scale population genomics studies effortlessly.

  • End-to-End Workflow: From sample preparation to advanced bioinformatics
  • Flexible Sequencing Depth: Tailored coverage options based on your study targets
  • Multi-Omic Integration: Seamlessly combine DNA, RNA, and single-cell datasets
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% RUN SUCCESS RATE
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FAQ’S

Have a question? We've got
the answers you need.

  • What are the sample submission and quality control (QC) requirements?
    We accept a wide range of biological samples, including genomic DNA, total RNA, fresh frozen tissue, and blood. Every incoming sample undergoes strict fluorometric and electrophoretic baseline quantification (QC) to ensure premium library preparation and sequencing output.
  • What is your standard turnaround time for Next-Generation Sequencing (NGS)?
    Our standard turnaround time is typically 2 to 4 weeks from the date your samples pass our initial Quality Control (QC) checkpoint. This timeline can vary slightly depending on the specific project scope, sequencing depth requirements, and whether customized bioinformatics analysis pipelines are requested. For time-sensitive studies, accelerated processing options may be available upon consultation.
  • What bioinformatics data formats do you deliver?
    We provide complete, publication-ready data delivery. By default, you will receive raw sequencing data in standard, high-fidelity FASTQ formats. For comprehensive projects, we also deliver fully mapped BAM/SAM alignment files, variant call files (VCF), and interactive, structured analysis reports (such as expression matrices or multi-QC summaries) via our secure cloud data portal.
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Consult Our Dedicated Genomics Support Specialists

24/7 Technical Support
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• ACCURACY • QUALITY • ARUNA MULTI-OMICS
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• SAMPLE • HIGH-THROUGHPUT NGS • BIOINFORMATICS
SERVICE WORKFLOW

Your Journey From Sample to
Actionable Data

01.

Sample Submission & QC

Submit your biological samples using our secure cold-chain logistics. Every sample undergoes strict initial quality control (QC) assessment.

02.

Library Preparation

Qualified samples are processed for library construction (DNA fragmentation, adapter ligation, and target enrichment) customized to your project specs.

03.

High-Throughput Sequencing

Libraries are loaded onto advanced NGS sequencers for deep parallel sequencing, generating raw data with guaranteed target Q30 metrics.

04.

Bioinformatics & Delivery

Raw FASTQ data is processed through automated pipelines. Access your comprehensive analysis reports and clean data via our secure cloud portal.

Looking for help? Contact us Today