The Run-Only Sequencing NGS Panel from Source Genomics is designed for researchers who have already prepared their libraries and need fast, accurate sequencing on Illumina NovaSeq, NextSeq, or MiSeq platforms. With unmatched flexibility in read modes, scalable outputs, and expert bioinformatics support, we ensure you receive the data you need with precision and efficiency.
Book a free consultation with our experienced scientists. Each project receives a dedicated account manager for end-to-end support throughout the project and post-data delivery.
Run-Only Sequencing NGS Panel
Our sequencing service is built to deliver high-quality results efficiently and reliably:
Quality Control (QC) Assessment
Evaluates the sequencing pool before the run to ensure sample integrity.
PhiX Spike-In
Enhances sequencing accuracy and increases pool diversity.
Full-Flow Cell Sequencing
Runs on Illumina NovaSeq, NextSeq, or MiSeq platforms for high-quality data generation.
Flexible Read Modes
Offers 100, 150, 200, 300, 500, and 600-cycle options to match your study’s needs.
Scalable Data Output
Produces between 1 million and 10,000 million reads per flow cell for projects of any scale.
Demultiplexed Data Return
Delivers sorted sequencing data securely via FTP transfer or HDD.
Optional Advanced Bioinformatics
Provides expert analysis, including de novo assembly, SNP and InDel analysis, and more.
Engineered for efficiency and adaptability, this approach ensures you receive high-quality sequencing data that integrates seamlessly into your workflows.
Custom Sequencing
Every sequencing study comes with its own challenges, from selecting target regions to optimising read depth. That’s why the Run-Only Sequencing NGS Panel from Source Genomics accommodates researcher-prepared libraries, including any custom NGS panel, allowing you to design and execute your sequencing projects without constraints.
By applying advanced sequencing technology and bioinformatics expertise, you can confidently analyse rare variants, monitor microbial diversity, or explore gene expression with data tailored to your exact specifications.
The Run-Only Sequencing Process
We’ve made the sequencing process as efficient as possible:
Submit Your Libraries
Send pre-prepared NGS libraries for sequencing.
Perform Quality Check (QC)
Assess the sequencing pool to ensure sample integrity.
Run Sequencing
Process libraries on Illumina NovaSeq, NextSeq, or MiSeq platforms using the selected read mode.
Demultiplex Data
Sort and format raw sequencing data for easy downstream analysis.
Deliver Secure Data
Provide high-quality, demultiplexed data via secure FTP transfer or HDD.
With precision-driven workflows and rigorous quality control, every sequencing run produces consistent, reproducible results.
Benefits
Our Run-only Sequencing NGS Panel is designed for flexibility, accuracy, and cost-effectiveness, giving you complete autonomy over your sequencing data.
High-Quality Data
Achieve precise and reproducible sequencing with advanced Illumina platforms.
Tailorable Read Modes
Choose the read lengths and sequencing depth that best suit your project.
Scalability
Generate anywhere from 1 million to 10,000 million reads per flow cell to match your study's needs.
Protected Data Access
Receive results through encrypted FTP transfer or HDD for seamless data retrieval.
Optional Bioinformatics Support
Access expert analysis services, including de novo assembly and SNP and InDel analysis.
Overview
Sequencing package details
As standard we offer entry QC of the provided sequencing pool, PhiX for sequencing QC and increased pool diversity, sequencing on full flow cells using the desired read mode and data output then return of the demultiplexed data via secure FTP server or HDD.
Sequencing instruments: Illumina NovaSeq, NextSeq and MiSeq
Sequencing read modes available: 100, 150, 200, 300, 500 and 600 cycles
- Example: 150bp paired end read mode uses 300 cycle reagents
- Custom read modes available e.g. 28r1 91r2
Sequencing outputs: 1 million to 10,000 million reads per flow cell
The process
We also offer advanced bioinformatics analysis packages as well as fully bespoke bioinformatics solutions.
For run-only projects, as standard we include the demultiplexing of raw data free of charge providing that library indexing information is provided. However, we can also utilise all relevant bioinformatics pipelines and we offer bespoke solutions if required.
A non-exhaustive list of possible bioinformatics analysis options is below:
- De novo genome assembly
- SNP and InDel analysis and annotation
- Trio/custom comparative analysis
- De novo transcriptome assembly
- Digital or differential gene expressions analysis
- Detection and quantification of gene-fusions and splice variants
- Metagenome taxonomic classification and differential abundance analysis
For a more in-depth discussion on our bioinformatics capabilities please contact your account manager or the bioinformatics team directly.
Genomics@sourcebioscience.com
How to order
Contact us today and one of our skilled account managers will be in touch with a free consultation including further information and pricing details.Â
Payment options:
Payment can be made by credit card or purchase order number.
FAQ's:
View our frequently asked questions for more information.Â
Sample requirements:Â
Please click here to view sample requirements.Â
Take Your Research Further with Trusted Sequencing
Let Source Genomics streamline your sequencing workflow with precision, speed, and seamless data integration. Reach out to us today to discuss your project and take the next step toward high-quality, reliable sequencing results.
Contact us today and one of our skilled account managers will be in touch with a free consultation including further information and pricing details.
Next Generation Sequencing
Source BioScience is one of Europe’s leading providers of commercial sequencing, offering Next Generation Sequencing services from our ISO accredited laboratories. We offer NGS services on the most prominent platforms including Illumina’s NovaSeq, NextSeq and MiSeq.