RNA-Seq Services

Fast, accurate, and cost-effective solutions tailored to your research needs

1. Unbeatable Pricing:

High-quality sequencing and get accurate results starting at $80/ sample

2. Rapid Turnaround

Faster results in just 1-3 weeks

3. Complete Transcriptome Insights

Comprehensive RNA Seq covering both mRNA and non-coding RNA analysis

4. AI-Driven Analysis

Gain powerful, intuitive insights with OmicsWeb AI

5. Minimal Sample Requirement

Process samples with as low as 10µL blood, 10ng RNA, or 1 FFPE slide

6. Low RIN compatibility

Samples with RIN as low as 2, unlike the typical requirement of RIN ≥ 5

Our Service

Price: starting at $80/ sample

Turnaround Time: 1-3 weeks

Analysis: AI-enhanced, comprehensive analysis

Sample Compatibility: works with RIN ≥ 2

Traditional Methods

Price: Expensive

Turnaround Time: 4-8 weeks

Analysis: Manual, time-consuming interpretation

Sample Compatibility: Requires RIN ≥ 5

We believe in clear, upfront pricing, so you know exactly what you’re paying for—no surprises. Get high-quality sequencing without the high cost.

Number of Samples

30-99

100-299

300-999

1000+

Price Per Sample

$110

$100

$90

$80

RNA Extraction Fee:

$20/sample (Cell/Blood)

$60/sample (Tissue/Other Types)

Submit samples across multiple projects
No expiration date until reaching 100 samples or $10,000 in value
Ideal for labs with flexible timelines or exploratory studies

Includes RNAseq services, raw FASTQ files, aligned gene count matrix, and full access to our OmicsWeb Copilot AI for advanced bioinformatics analysis.

*This promotion is available to nonprofit institutions

how it worksRapid Turnaround: From Sample to Discovery in 1-3 weeks

Fast and Flexible

Standard delivery in 15business days from just $80/sample

Need it Sooner?

Priority express option delivers results in just 7 days

Streamlined Workflow

From quote to data in 4 simple steps

End-to-End Service

We handle RNA extraction, library prep, sequencing, and analysis

Ready-to-Use Results

Access FASTQ files, gene counts, and insights on OmicsWeb with AI-powered co-pilot

Beyond mRNA:

Capture the full transcriptome—including non-coding RNAs—for deeper biological insights

Smarter Sequencing:

Eliminate rRNA bias using our proprietary PERD technology

More for Less:

Achieve 16x higher throughput and cut sequencing costs by up to 90%

Future-Ready:

Ideal for challenging samples, tight budgets, and precision applications in research, pharma, and diagnostics

1. Low Output, High Impact:

Process samples with as little as 10 µL of blood, 10 ng of RNA, or 1 FFPE slide

2. Flexible Sample Types:

Compatible with plasma, serum, whole blood, FFPE, fresh frozen tissues, PBMCs, cell lines, etc.

3. Validated Technology:

Proven performance with RIN ≥ 2 — ideal for degraded, precious samples or historical samples

4. Built for Precision:

BIRT technology ensures high-quality RNA-seq results, even from ultra-low input volumes

5. Versatile Applications:

Optimized for both discovery research and clinical sample profiling across oncology, immunology, and other diseases

1. RIN ≥ 2 Ready:

Confidently process degraded RNA samples with RIN as low as 2, unlike conventional protocols that require RIN ≥ 5

2. FFPE-Friendly:

Ideal for archival and clinical specimens where RNA integrity is often compromised

3. Powered by BIRT:

Barcode-Integrated Reverse Transcription ensures robust cDNA generation from fragmented RNA

1. More Data, Less Waste:

Maximize data recovery from low-quality or limited samples without sacrificing accuracy

2. No Enzyme Bias:

Combined with PERD, our non-enzymatic depletion workflow preserves transcript integrity across RNA quality levels

"Partnering with BioState AI has been a game-changer for our research. Their platform is not only incredibly powerful but also intuitive and adaptable to the unique needs of our projects. What truly sets them apart is their commitment to scientific rigor paired with cutting-edge machine learning—helping us accelerate discovery without compromising on quality or insight. The team is responsive, deeply knowledgeable, and genuinely invested in our success. With BioState AI, we’re not just accessing tools—we’re gaining a strategic partner in innovation.”

Hunter EdwardsPh.D., NemaLife, Inc.

Biostate AI's customer support has been outstanding—they were responsive, knowledgeable, and made the entire process hassle-free. Their BIRT technology is also incredibly cost-effective, providing high-quality RNA-seq results without breaking the budget. What really stood out was the integration with OmicsWeb Copilot—it made data analysis so much easier. Instead of spending weeks manually processing and interpreting results, I was able to dive deep into the data with just a few clicks. OmicsWeb Copilot provided clear insights, helped identify key patterns, and ultimately saved me a lot of time and resources. It’s a game-changer for RNA-seq analysis!"

Xiaonan HanPrincipal Investigator, Hematology/Medical Oncology, Case Western Reserve University

Working with Biostate AI has been a great experience. The entire process—from data delivery to analysis—has been seamless. Having pre-aligned read counts made it incredibly easy to get started, and OmicsWeb Copilot has been a game-changer in our analysis. It helps dive deeper into the data, saving us a significant amount of time and resources. We’re excited about the insights we’re uncovering and look forward to future collaborations!”

Kyle FinkPrincipal Investigator, Neurology, UC Davis

Happy clients

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Key FeaturesUnlock Deeper Gene Insights with AI-Enhanced Total RNA Sequencing

Fast, accurate, and cost-effective solutions tailored to your research needs

Pricing Comparison

biostate AI price cardTransparent Pricing: No Hidden Costs

We believe in clear, upfront pricing, so you know exactly what you’re paying for—no surprises. Get high-quality sequencing without the high cost.

40% OFF!!

$6000 for $10,000 RNAseq value (up to 100 samples)

Fast and Flexible

Need it Sooner?

Streamlined Workflow

End-to-End Service

Ready-to-Use Results

servicesComplete Transcriptome Insights with BIRT+PERD

Beyond mRNA:

Smarter Sequencing:

More for Less:

Future-Ready:

Minimal Sample Requirement: Do More with less

servicesLow RIN Compatibility: Reliable Results from Challenging Samples

capabilitiesAI-Driven Insights with OmicsWeb

1. Expert Optimization:

2. Talk to Your Data:

3. Generate code:

4. Data Transformation:

DownloadBIRT+PERD White Paper

TestimonialsWhat Our Customers and Partners Say

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