Starting at $130/sample - Whole Genome Sequencing with Free Basic Bioinformatics included

Our facility offers whole genome sequencing for a comprehensive analysis of bacterial, viral, yeast, and phage genomes. This is great for research and studies in public health, epidemiology, diseases, and pharmacology. Our average turnaround time is 10-15 business days, accelerating your research by months.

Pricing includes DNA extraction, samples QC, library preparation, genome sequencing, bioinformatics, and data storage.

We offer a wide variety of sequencing panels that can be used for the following research applications:

• Genomics in Drug Development / Pharmacology
  
• Immuno-oncology
  
• Immunology
  
• Microbial Genomics
  
• Cellular and Molecular Research
  
• Complex Disease Genomics
  
• Forensic Genomics
  
• Genetic Health
  
• Argigenomics
  
• Neuroscience
  
• Oncology
  
• Reproductive Health
  
• Transplant Genomics

Starting at $130/sample - Whole Genome Sequencing with Free Basic Bioinformatics included

Our facility offers whole genome sequencing for a comprehensive analysis of bacterial, viral, yeast, and phage genomes. This is great for research and studies in public health, epidemiology, diseases, and pharmacology. Our average turnaround time is 10-15 business days, accelerating your research by months.

Pricing includes DNA extraction, samples QC, library preparation, genome sequencing, bioinformatics, and data storage.

We offer a wide variety of sequencing panels that can be used for the following research applications:

• Genomics in Drug Development / Pharmacology
  
• Immuno-oncology
  
• Immunology
  
• Microbial Genomics
  
• Cellular and Molecular Research
  
• Complex Disease Genomics
  
• Forensic Genomics
  
• Genetic Health
  
• Argigenomics
  
• Neuroscience
  
• Oncology
  
• Reproductive Health
  
• Transplant Genomics

Starting at $350/sample - High resolution HLA-Typing with rapid turnaround time

Gain high resolution sequencing data from 11 HLA loci through our HLA typing sequencing. HLA genes are a major factor in the immune response system and are often associated with autoimmune disorders or infectious diseases. HLA typing provides critical insight into these gene functions.

Pricing includes everything from sample handling, sample extraction, QC, library prep, sequencing, and basic bioinformatics. Pricing varies based on panel.

When performing HLA typing with The Sequencing Center, you can expect to receive results in 72 hours with both raw and variant data in a comprehensive report. We perform the HLA typing on our Next Generation Sequencing Illumina MiniSeq. This system is capable of sequencing up to 7.5 Gb with a read length of 2 x 150 bp.

The Sequencing Center offers highly affordable library preparation services for small genomes, amplicons, and plasmids with turnaround times measured in days instead of weeks.

Our kits support a wide variety of DNA input, starting at just 1ng of DNA. With the ability to scale up to hundreds of samples in a single run, our customers get the benefit of preparing large quantities of samples in short timeframes through our automated facility.

Turnaround time is typically ~3-5 business days.

The Sequencing Centers offers DNA extraction services for a wide variety of sample types, including blood, tissue, and cells from human, animal, yeast, bacteria, and viruses. Our service provides high quality and automated DNA extraction for an affordable price.

Our typical turnaround time is ~2-5 business days. Pricing excludes shipping costs.

Starting at $130/sample - Targeted Cancer Gene Panels for a Highly Affordable Price

The Sequencing Center offers many targeted sequencing panels designed to focus on various cancers. These panels range from targeting just 15 of genes to thousands.

Pricing includes everything from sample handling, sample extraction, QC, library prep, sequencing, and basic bioinformatics. Pricing varies based on panel.

Cancers included, but not limited to, in this list are:
- Colorectal Cancer
- Lung Cancer
- Breast Cancer
- Gastric Cancer
- Ovarian Cancer
- Melanoma Cancer

Starting at $130/sample - Affordable targeted gene panels for a variety of research applications

Amplicon Cancer Panel enables researchers to detect mutations with high sensitivity for genes commonly associated with different types of cancer.

Custom Targeted Sequencing Panel designed to target any number of genes our clients need. We work closely with researchers on developing custom panels for clinical research, pharmacology, and academic applications.

Starting at $130/sample - Affordable targeted gene panels for a variety of research applications

Amplicon Cancer Panel enables researchers to detect mutations with high sensitivity for genes commonly associated with different types of cancer.

Custom Targeted Sequencing Panel designed to target any number of genes our clients need. We work closely with researchers on developing custom panels for clinical research, pharmacology, and academic applications.

Starting at $77/sample - Targeted Breast Cancer Gene Panel for a highly affordable price

The Sequencing Center offers a targeted Breast Cancer Gene Panel for clinical researchers based on 26 genes. These genes are specified by NIH NLM Breast Cancer as contributing genes. NIH identifies six genes as “high penetrance”, as they are associated with high risk patients. They also identify an additional 20 genes as “moderate” or “low” penetrance. Collectively, these 26 genes yield a definitive risk profile for breast cancer patients.

This panel targets the exons for these 26 genes, providing high sequencing coverage for genes related to breast cancer.

Pricing includes everything from sample handling, sample extraction, QC, library prep, sequencing, and basic bioinformatics. Pricing varies based on panel.

Starting at $250/sample - Targeted Tumor Profiling for oncology research

Our facility offers over 20 different tumor profiling panels covering a wide range of oncology research areas.

Our panels have the capabilities to cover tumor profiles such as:
- Acute myeloid leukemia (AML)
- Myelodysplastic syndrome (MDS)
- Myeloproliferative neoplasms (MPN)
- Chronic myelogenous leukemia (CML)
- Chronic myelomonocytic leukemia (CMML)
- Juvenile myelomonocytic leukemia (JMML)

Additionally, we provide panels that offer insights into:
- Gene fusions
- Novel transcriptions
- Somatic mutations
- Transcript variants
- Chromosomal abnormalities
- Germline mutations
- Insertions/Indels
- Short tandem repeats
- Single nucleotide polymorphisms
- Structural variants

Pricing includes everything from sample handling, sample extraction, QC, library prep, sequencing, and basic bioinformatics. Pricing varies based on panel.

Starting at $400/sample - Target 552 inheritable disease genes

We offer an inherited disease sequencing panel that targets 552 genes associated with severe, recessive pediatric onset diseases.

This panel can identify germline mutations and SNPs with the ability to do deeper post-sequencing analysis through bioinformatics.

Pricing includes everything from sample handling, sample extraction, QC, library prep, sequencing, and basic bioinformatics. Pricing varies based on panel.

Each engagement includes a comprehensive summary, actionable insights, raw data, and reproducible results. All files are transferred over secure methods.

Our expert bioinformatics teams utilizes leading methodologies to produce accurate, high quality, and reproducible results. Our facility leverages the latest bioinformatics software to provide accurate and clear analysis for each client. Clients that work with us enjoy an in depth and clear summary of their sequenced data with direct access to the raw data, variant data, a comprehensive report, and a steps to reproduce results.

Some of the NGS pipelines we offer
- Sequence Assembly and Assembly
- Comparative Genomics
- Protein and Interactome Pathways
- Proteomics
- DNA-Seq
- RNA-Seq
- CHiP-Seq
- Ribo-Seq
- Methyl-Seq
- Metagenomics
- De novo Assembly
- Pathway Analysis

Let us worry about storing your data securely so that you can get back to your research.

The most overlooked step in genome sequencing is handling the torrent of data that is produced on each run. A typical bacterial WGS can produce over 20GB of data, causing exploding data management costs and complexity. At The Sequencing Center, we provide managed genome data storage and analytics that allows users to easily scale to their research needs.

Our fully managed data storage solution provides you with peace of mind knowing that we take care of all of the heavy lifting. There are no lock-in contracts and you can increase, decrease or cancel your plan at any time.

Tiers:
- 600GB = $40/mo
- 2TB = $150/mo
- 10TB = $810/mo
- 50TB = $1,200/mo
- 1PB = $10,500/mo