DNA Library Sequencing Services
THE FOUNDATION OF ALL NGS LIBRARY PREPARATION
DNA library sequencing services prepare DNA fragments for sequencing. SeqMatic offers DNA sequencing solutions for a wide-range of applications related to genomics, transcriptomics, epigenomics and a multitude of other omics for any organism. Variations in NGS methods come from sample preparation and analysis options.
Learn about SeqMatic’s most popular applications for DNA library sequencing services:
Service Features
- Expert pooling validated by MiSeq Nano – to ensure equal sample distribution
- Proprietary TailorMix PhiX control – For reducing cross-talk during data processing and analysis
- Scalability from pilot to production – One partner for any scale project – equipped to support any size project – no sample minimum or maximum!
- All DNA projects are performed in a CLIA environment – To ensure consistent quality

Service Highlights
Comprehensive Services – Complete DNA workflow, including extraction from virtually any sample type, library generation, sequencing, and data analysis services
Prepare Libraries From Difficult Samples – Low input DNA (as low as 1ng), blood, blood cards, saliva, stool, environmental samples, cell-free DNA and FFPE
Stringent Quality Controls – All sample preparation and library construction steps are validated by multiple assays (Qubit, TapeStation, qPCR and test sequencing)
Fast Turnaround Time – Standard and Express Services available
Technical Support – QC reports prepared for review by the customer to decide which samples qualify for library preparation, or alternative library preparation/sample re-submission
Flexibility – Choice for sample processing: manually or automated using a wide-range of processing technologies
Wide-Range of Sample Types – human, animal, fish, plant, bacteria/fungi, environmental, viruses/phages from virtually any source
If you have DNA – we can sequence it!
The determination of the exact sequence of nucleotides or bases, in a DNA molecule enables researchers and scientists to:
- learn more details about human genetic variation
- screen new treatments and therapies
- prepare for genetic research projects
- identify the genetic causes of diseases
- study human evolution
The SeqMatic Difference
Expert NGS
The SeqMatic approach starts with proven genomic workflows and proprietary controls that have been refined and optimized over the past decade to deliver considerably more data than Illumina specifications.
Expert NGS
The SeqMatic approach starts with proven genomic workflows and proprietary controls that have been refined and optimized over the past decade to deliver considerably more data than Illumina specifications.
View MoreConscientious Attention To Detail
We learn about the goals of our customer’s scientific research and the type of sequencing data that would be most beneficial to their project.
Conscientious Attention To Detail
We learn about the goals of our customer’s scientific research and the type of sequencing data that would be most beneficial to their project.
View MoreTailor-made Services with Fast TAT
Then we modify our workflow to target those specific reads. Couple that effort with world class turnaround time.
Tailor-made Services with Fast TAT
Then we modify our workflow to target those specific reads. Couple that effort with world class turnaround time.
View MoreOptimal Solutions to Research Needs
This application of best science, higher quality data, more read depth per lane, and fast delivery makes SeqMatic an exceptional partner and value per research dollar spent.
Optimal Solutions to Research Needs
This application of best science, higher quality data, more read depth per lane, and fast delivery makes SeqMatic an exceptional partner and value per research dollar spent.
View MoreGet Your Results
Optimal solutions are custom-made according to research needs




Pre-Submission
Planning & Consultation - Assurance of de-identified sample submission and handling
Sample Submission
Nucleic Acid Extraction - We accept a wide range of sample types
Library Preparation
Library Generation - Amplified cDNA is used for sequence libraries' construction
Sequencing
Different platforms for different data outputs
Data Analysis
Custom BioInformatics