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Fully automatic parallel peptide synthesizer

Sequencing Only

Ready-to-Sequence Libraries. Flexible Sequencing Solutions.

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Home Services Sequencing Services NGS Sequencing Only

Overview

Quintara Sequencing Only provides a cost-effective solution for researchers who prepare their own sequencing libraries. We handle sequencing and demultiplexing, with flexible sequencing options to support a wide range of applications, including WGS, RNA-seq, amplicon sequencing, ATAC-seq, CUT&RUN, and single-cell sequencing. Get the sequencing data you need without the added cost of library preparation.

Flexible Options
Multiple Read Lengths & Data Outputs
Easy Submission
1000+ Free Drop Boxes
Reliable Quality Control
Library QC Before, Data QC After
More Savings
Capacity-Based Discounts

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Workflow

From library submission and pre-sequencing QC to flexible sequencing and data delivery, Quintara Seq-Only streamlines your sequencing workflow. Customize read length and data output, optionally add PhiX spike-in, and receive raw sequencing data with QC reports and optional downstream data analysis to support your research.

Library Submission

Submit Your Ready-to-Sequence Libraries
Library QC

Quality Checks Before Sequencing
Sequencing

Flexible Read Lengths, Read Pairs & Optional PhiX
Data Delivery

Raw Data & Optional Downstream Analysis

Services

Read Length	Read Pairs	Price +
2 x 75 bp	20 M – 1000 M	Starting from $100
28 bp + 90 bp	20 M – 1000 M	Starting from $100
2 x 150 bp	20 M – 1000 M	Starting from $150
2 x 300 bp	0.5 M – 400 M	Starting from $140

* Turnaround time may vary depending on sequencing capacity and scheduling. Contact us for the most accurate timeline.

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FAQ

What are the requirements for i5 and i7 index sequences?: The i5 and i7 index sequences must each be 10 bp long. If your indexes are shorter than 10 bp, please add the appropriate number of padding bases from the adjacent primer sequence so that each index read totals 10 bp. Please confirm that your index sequences and padding bases are compatible with the sequencing configuration.

Will adding PhiX affect the number of reads I receive?: Yes. PhiX control consumes sequencing capacity and will reduce the number of reads allocated to your library. Please consider this when selecting your sequencing output. PhiX spike-in is optional and should be selected based on your library type and sequencing requirements.

What is the difference between read pairs and total reads?: One read pair = 2 reads. For paired-end sequencing, each read pair consists of one forward read (R1) and one reverse read (R2). For example, 20 M read pairs = 40 M total reads. The total number of bases also depends on the selected read length.

What data and reports will I receive?: You will receive raw sequencing data in FASTQ format and applicable sequencing QC reports. Demultiplexed FASTQ files are provided when applicable. Optional downstream data analysis may also be available depending on your application and analysis requirements.

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