Novogene provides cost‑effective sequencing‑only services for customer‑prepared, ready‑to‑sequence libraries on the state‑of‑the‑art NovaSeq X Plus platform. With a flexible portfolio of sequencing solutions, we offer multiple read lengths, throughput options, and turnaround times to support a wide range of research needs and project scales.
Our Swift Sequencing for Premade Libraries delivers a faster, more cost-effective sequencing solution for ready-to-sequence, pooled libraries. Need a faster turnaround? Try Swift to get your data sooner.
Access some of the most competitive sequencing costs on a per-read/per-Gb basis, with a guaranteed Q30 ≥ 85% for high-quality data you can trust.
Rely on Novogene’s experienced team for seamless project handling, technical guidance, and consistent, high-quality sequencing output from start to finish.
Benefit from rapid, no-extra-fee turnaround, enabling quick progress from library submission to data delivery within 1-2 weeks.
Buy by the lane or by the data amount. Support for a broad range of library types, and customizable sequencing parameters sequencing parameters.
Enjoy convenience and faster logistics with Novogene’s local laboratory operations across the USA (Davis, CA, and Beaverton, OR)
Experience streamlined project execution through Novogene’s Customer Service System (CSS), enabling efficient data management and communication throughout the sequencing process.
High-throughput sequencing of customer-prepared libraries empowers a wide range of research workflows with maximum flexibility, efficiency, and control.
Generate consistent, high-volume sequencing output for population genetics, clinical research, screening projects, and large cohort studies that require scalable and reliable data generation.
Obtain high-quality raw sequencing data designed for seamless integration into your in-house analysis workflows, giving you full control over data processing, interpretation, and downstream analytics.
Combine your preferred library preparation methods with Novogene’s high-capacity sequencing to optimize costs, streamline resources, and customize your NGS workflow end-to-end.
Enable flexible data generation for genomics, transcriptomics, targeted sequencing, metagenomics, and other NGS-based applications that rely on accurate, scalable sequencing-only solutions.
Our Partial Lane Sequencing service allows multiple projects to share a lane on the NovaSeq X Plus, offering multiple buckets of 50 Gb, 100 Gb, 150 Gb, 200 Gb and larger volumes available. Your libraries are expertly grouped and balanced with other samples to ensure optimal base diversity on the lane, eliminating the need for PhiX spike-in libraries as balancers and maximizing usable lane space.
Our Full Lane Sequencing service offers entire lanes of the flow cell on NovaSeq X Plus for exceptional throughput and sequencing consistency. By minimizing cross-contamination risks, the Full Lane Sequencing ensures reliability and precision of your sequencing results.
To maintain high-quality data from NovaSeq X Plus, it’s essential to preserve base diversity on the lane. We recommend selecting index adapters with diverse index sequences that optimize color balance within pooled libraries. This strategy is essential for successful demultiplexing and subsequent data analysis.
You can request a quote through our online e-commerce platform or contact a Novogene representative to discuss your project. Before shipping your premade libraries, submit the required sample information through our CSS system to ensure smooth project processing.
Upon arrival, your libraries will undergo quality assessment. A library QC report, including mass concentration, molar concentration, fragment size, and library grade, will be available in CSS for your review and confirmation before sequencing proceeds.
Approved libraries are pooled based on their effective concentrations and ordered data volumes, then sequenced on the NovaSeq X Plus platform. The resulting data are demultiplexed and quality-controlled. Your sequencing data and data QC report will be delivered with support from your dedicated Novogene representative.
Quality score distribution across sequencing cycles, reflecting overall base-calling accuracy along read positions.
Base error rate across read positions, illustrating sequencing accuracy and quality stability along the read length.
Base composition distribution (A, T, G, C) across sequencing cycles to evaluate potential sequence bias.
Summary of raw read filtering results, showing proportions of clean reads, adapter-related reads, and other read categories.
We can sequence Illumina-compatible libraries that contain standard Illumina adapter and sequencing primer binding regions and can be sequenced using standard Illumina workflows. Most commercial library preparation kits are Illumina-compatible. Feel free to contact us if you need support.
Our platform offers tailored solutions for
your unique experimental needs, ensuring a seamless experience from project design to data delivery.
Novogene provides cost‑effective sequencing‑only services for customer‑prepared, ready‑to‑sequence libraries on the state‑of‑the‑art NovaSeq X Plus platform. With a flexible portfolio of sequencing solutions, we offer multiple read lengths, throughput options, and turnaround times to support a wide range of research needs and project scales.
Our Swift Sequencing for Premade Libraries delivers a faster, more cost-effective sequencing solution for ready-to-sequence, pooled libraries. Need a faster turnaround? Try Swift to get your data sooner.
Access some of the most competitive sequencing costs on a per-read/per-Gb basis, with a guaranteed Q30 ≥ 85% for high-quality data you can trust.
Rely on Novogene’s experienced team for seamless project handling, technical guidance, and consistent, high-quality sequencing output from start to finish.
Benefit from rapid, no-extra-fee turnaround, enabling quick progress from library submission to data delivery within 1-2 weeks.
Buy by the lane or by the data amount. Support for a broad range of library types, and customizable sequencing parameters sequencing parameters.
Enjoy convenience and faster logistics with Novogene’s local laboratory operations across the USA (Davis, CA, and Beaverton, OR)
Experience streamlined project execution through Novogene’s Customer Service System (CSS), enabling efficient data management and communication throughout the sequencing process.
High-throughput sequencing of customer-prepared libraries empowers a wide range of research workflows with maximum flexibility, efficiency, and control.
Generate consistent, high-volume sequencing output for population genetics, clinical research, screening projects, and large cohort studies that require scalable and reliable data generation.
Obtain high-quality raw sequencing data designed for seamless integration into your in-house analysis workflows, giving you full control over data processing, interpretation, and downstream analytics.
Combine your preferred library preparation methods with Novogene’s high-capacity sequencing to optimize costs, streamline resources, and customize your NGS workflow end-to-end.
Enable flexible data generation for genomics, transcriptomics, targeted sequencing, metagenomics, and other NGS-based applications that rely on accurate, scalable sequencing-only solutions.
Our Partial Lane Sequencing service allows multiple projects to share a lane on the NovaSeq X Plus, offering multiple buckets of 50 Gb, 100 Gb, 150 Gb, 200 Gb and larger volumes available. Your libraries are expertly grouped and balanced with other samples to ensure optimal base diversity on the lane, eliminating the need for PhiX spike-in libraries as balancers and maximizing usable lane space.
Our Full Lane Sequencing service offers entire lanes of the flow cell on NovaSeq X Plus for exceptional throughput and sequencing consistency. By minimizing cross-contamination risks, the Full Lane Sequencing ensures reliability and precision of your sequencing results.
To maintain high-quality data from NovaSeq X Plus, it’s essential to preserve base diversity on the lane. We recommend selecting index adapters with diverse index sequences that optimize color balance within pooled libraries. This strategy is essential for successful demultiplexing and subsequent data analysis.
You can request a quote through our online e-commerce platform or contact a Novogene representative to discuss your project. Before shipping your premade libraries, submit the required sample information through our CSS system to ensure smooth project processing.
Upon arrival, your libraries will undergo quality assessment. A library QC report, including mass concentration, molar concentration, fragment size, and library grade, will be available in CSS for your review and confirmation before sequencing proceeds.
Approved libraries are pooled based on their effective concentrations and ordered data volumes, then sequenced on the NovaSeq X Plus platform. The resulting data are demultiplexed and quality-controlled. Your sequencing data and data QC report will be delivered with support from your dedicated Novogene representative.
Quality score distribution across sequencing cycles, reflecting overall base-calling accuracy along read positions.
Base error rate across read positions, illustrating sequencing accuracy and quality stability along the read length.
Base composition distribution (A, T, G, C) across sequencing cycles to evaluate potential sequence bias.
Summary of raw read filtering results, showing proportions of clean reads, adapter-related reads, and other read categories.
We can sequence Illumina-compatible libraries that contain standard Illumina adapter and sequencing primer binding regions and can be sequenced using standard Illumina workflows. Most commercial library preparation kits are Illumina-compatible. Feel free to contact us if you need support.
Our platform offers tailored solutions for
your unique experimental needs, ensuring a seamless experience from project design to data delivery.
