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PCR Amplicons & Plasmid Sequencing Services

Sequence dozens to hundreds of PCR amplicons at once from any source

Amplicon sequencing enables the profiling of PCR products with ultra-high read-depth and high-throughput.

Service Highlights

PCR Amplicon Sequencing

  • Library Preparation services available
  • Long amplicons can be sequenced at full length using MiSeq 500 and 600 cycle kits and the NovaSeq SP500
  • NovaSeq 6000 and NovaSeq X are available for high-throughput projects (up to 384 unique samples)
  • TailorMixTM Indexed PhiX controls to address low diversity
  • Consultation for staggered sequencing to maximize diversity by request
  • Your validated custom primers can be used for two-step PCR or during sequencing

Fast Turnaround Time

  • 3 to 5 business days Express Service for prepared libraries
  • 10 business days Express Service for library preparation
  • Pooling and Normalization of pre-made libraries are available
Service Features

Stringent Quality Controls

SeqMatic qualifies DNA with a TapeStation Electropherogram and Qubit for each total DNA sample submitted. A TapeStation analysis includes a DNA Integrity Number (DIN) for each sample, where a value of 10 indicates a perfectly intact sample and a value of 1 indicates a severely degraded sample. Results are shared for review and approval prior to proceeding to library preparation.

High-Quality Design Considerations for Read Depth

SeqMatic offers typical read depth of 50K to 100K or more reads per sample. Higher and lower read depths are available depending on project needs.

Preliminary Sequencing

After library preparation, libraries are pooled in equal volumes and the final pool is quantified by Agilent TapeStation and checked via preliminary sequencing (MiSeq). Libraries are then normalized and re-pooled based on the read counts from the preliminary sequencing dataset.

World-Class Validation Standards & Practices

SeqMatic is equipped to ensure accurate, repeatable, and reproducible results. SeqMatic’s quality program has been audited and approved as part of becoming a Clinical Laboratory Improvement Amendments (CLIA) and College of American Pathologists (CAP) certified sequencing facility.

Our CLIA quality program requires the use of well-defined protocols to maintain the consistency and reproducibility of our NGS workflows. Thus, samples are processed in a CLIA environment.

Custom Assay Services

Our highly personalized sequencing services can be adapted to almost any high- and/or low-throughput sequencing workflow required by our customers so that we optimize the quality and quantity of data output.

  • DNA Encoded Libraries (DEL)
  • BCR and TCR profiling
  • Affinity Maturation
  • CRISPR target validation
  • Genotype assays
  • SNP detection
  • High-throughput metagenomics
  • Custom amplicon solutions

Doski, Shadin, et al. “Complete sequence and genome characterization of a new potexvirus isolated from Chaenostoma cordatum.” Archives of Virology 167.10 (2022): 2089-2092.
Cervantes, Jorge, et al. “Investigation of oral, gastric, and duodenal microbiota in patients with upper gastrointestinal symptoms.” Journal of Investigative Medicine 69.4 (2021): 870-877.
Gavrili, Vasileia, et al. “First report of barley virus G infecting corn in Greece.” Journal of Plant Pathology 103 (2021): 1331-1331.
Leung, Marcus HY, et al. “Changes of the human skin microbiota upon chronic exposure to polycyclic aromatic hydrocarbon pollutants.” Microbiome 8.1 (2020): 1-17.
Wintermantel, W. M., et al. “First report of Cucurbit chlorotic yellows virus infecting melon in the New World.” Plant Disease 103.4 (2019): 778-778.
Find other Research Publications from around the world!

Service Portfolio

PRODUCT HIGHLIGHT

TailorMix Dual-Indexed PhiX