US Based · Single Cells & Trace Inputs

Ultra-Low Input RNA Sequencing Service

High-sensitivity transcriptomic data from trace samples — rare cell populations, laser capture microdissection, and liquid biopsies. Takara SMART-Seq chemistries run end-to-end in our SF Bay Area lab.

At a glance

Library prep

Takara SMART-Seq mRNA

RNA input

10 pg–10 ng, 1–1,000 cells

Sequencing

NovaSeq X+ PE150

Read depth

20M paired reads

Turnaround

Expedited available

Price

$250/sample
Volume pricing available

Service Highlights

From low input RNA to results, all in one lab

Send sorted cells, lysates, or purified RNA. Every stage is performed in-house with defined QC criteria and validated Takara SMART-Seq chemistry built for trace inputs.

Extraction & Sample QC

Extraction & Sample QC

Library prep

Library prep

Sequencing

Sequencing

Analysis

Analysis
Sample Requirements

Check your sample compatibility

Oligo-dT capture validated for human, mouse and rat, and adaptable to any eukaryote with polyA transcripts.

Sample type SAMPLE REQUIREMENTS
Purified RNA Preferred 10 ng in 15 µl, RIN >7
Lowest limit 10 pg in 15 µl, RIN >7
Sorted cells >10,000 cells for extraction
50–1,000 in lysis buffer for direct input
Tissue Small flash-frozen pieces, e.g. 3 mm punch biopsies
Micro-dissected tissue (LCM) Captured structures collected directly into approved lysis buffer and flash-frozen immediately. No column extraction.
Aspirates & biofluids Fine needle aspirates, or plasma and serum for cfRNA. Contact us for volume guidance and plasma processing requirements.
Alternative workflows

Have higher input, degraded or few cells? Your samples may be compatible with other services.

Technical excellence

Built for degraded and cross-linked RNA

Sort intact cells straight into our validated lysis buffer and flash-freeze. Skipping column extraction avoids the adsorption losses that destroy trace samples before prep even begins.
Fluorometric Qubit quantification and Fragment Analyzer sizing are run on micro-volume inputs, and you receive both reports before library construction. If a sample misses threshold, your project manager reviews options with you first.

Automated liquid handling removes operator variance, so your samples stay comparable — whether that is eight or eight hundred.

Oligo-dT priming selectively captures mature polyadenylated mRNA from pristine inputs down to 10 pg, so ribosomal and other non-polyadenylated RNA is simply never primed. Full-length coverage across each transcript, with no separate depletion step to lose material.
Template switching with locked nucleic acid modifications amplifies only full-length transcripts, preserving true proportions without the 3′ or 5′ bias that distorts trace-input libraries.

Illumina NovaSeq X Plus with PE75 or PE150 chemistry. 10–20M reads suits expression profiling and clustering; 30–50M for deep clinical or transcription factor work; 70M+ for rare splicing and lncRNA discovery.

Service experience

Working with us

Every project is run by scientists, tracked in one portal, and processed entirely in our own lab.

PhD-Level Project Oversight

A PhD scientist owns your project from design through interpretation.

Dedicated Project Manager

One point of contact from quote through delivery.

Easy Ordering

Register samples, track status, and download results in one portal.

100% US-Based

Every stage runs in-house in Foster City, CA. No outsourcing.

Resources & insights

Technical resources

Frequently asked questions

Planning your low-input project

Samples & service

Intact isolated cells, cell lysates, clinical fine needle aspirates, micro-dissected tissue, and plasma or serum biofluids. Our team will guide you to the right collection and lysis protocol for your material.

Yes. Sorting intact cells directly into our validated lysis buffer and flash-freezing immediately is our preferred method — it avoids the severe nucleic acid adsorption losses common to column extraction.

Human, mouse and rat are fully validated. Any eukaryote with polyadenylated transcripts and a reference genome can be supported — contact us to discuss your organism.

Takara SMART-Seq mRNA, an oligo-dT primed full-length chemistry built for ultra-low input. If your material is degraded or you need non-coding RNA, that runs on a different workflow — see our degraded and FFPE RNA-Seq service.

Data & delivery

10–20M reads per sample covers cost-effective profiling and standard differential expression. 30–50M expands the dynamic range for deep clinical expression and transcription factor work. 70M+ suits alternative splicing, low-abundance transcripts, and isoform discovery.

Starting from picogram-level RNA requires extra PCR cycles to reach clustering thresholds, which naturally generates duplicates. Our pipelines incorporate UMIs and custom metrics to separate that sequencing noise from genuine biological signal.
Your data is available on our secure FTP for 2 weeks after delivery, and we retain it in storage for 60 days. Extension options are available — ask your project manager, or request a direct transfer to your own AWS, Globus, or cloud storage.

Yes. Analysis can be added any time. If within the 60-day data retention window you will not need to resubmit the data. Contact your project manager and we will quote the additional analysis.

Ordering & logistics

Submit your inquiry below and our team will help create an account and walk you through submitting your samples.

Register your samples in the customer portal to generate your shipping documents, then print them and include them in your package. All samples should be shipped on dry ice overnight, or you can schedule a local same-day courier in the SF Bay Area.

Standard turnaround is 3 to 4 weeks from the day your samples pass incoming QC to final data delivery. Expedited processing is available on every order, in 10 to 14 business days — just ask your project manager.

There is no order minimum. We do recommend at least three biological replicates per condition for reliable differential expression, and per-sample pricing improves with batch size.

Get started with your project

Ready to accelerate your transcriptomic research? Contact our team for a technical consultation. We will guide you through low-input sample requirements and direct sorting options aligned to your analysis goals.

Request a quote