At GENXMAP, we offer a comprehensive suite of sequencing services tailored to meet the diverse needs of research, clinical, and industrial applications. Leveraging the latest in sequencing technologies, we provide precise, high-throughput, and versatile solutions to help you achieve your research goals. Our services include Sanger Sequencing, NovaSeq 6000, MiSeq, and Oxford Nanopore Technology (ONT), each with distinct advantages for different project requirements.

 

1. NovaSeq 6000 Service

 

• Overview:

Our NovaSeq 6000 service offers state-of-the-art, high-throughput sequencing designed for the most demanding genomic projects. This platform is perfect for large-scale studies, providing comprehensive genomic insights at an unprecedented scale.

 

• Advantages:

- Scalability: Capable of sequencing up to 6 terabases in a single run, suitable for extensive genomic projects.

- Flexibility: Multiple flow cell options allow customization based on project size and complexity.

- Cost-Effective: Reduced cost per base for large-scale projects, maximizing research budgets.

 

• Applications:

- Whole-Genome Sequencing (WGS): Uncover genetic variations and disease mechanisms through complete genome analysis.

- Exome Sequencing: Target coding regions to identify variants associated with diseases.

- Transcriptomics: Perform large-scale RNA sequencing, including single-cell RNA-Seq for gene expression analysis.

 

2. MiSeq Service

 

• Overview:

Our MiSeq service is ideal for smaller-scale sequencing projects requiring rapid turnaround times and high accuracy. It is perfect for targeted sequencing and smaller genome projects where precision and speed are essential.

 

• Advantages:

- Rapid Turnaround: Quick run times enable timely results for urgent projects.

- Versatility: Supports a broad range of applications, from amplicon sequencing to small genome sequencing.

- High-Quality Data: Reliable accuracy makes it a trusted choice for clinical diagnostics and targeted research.

 

• Applications:

- Targeted Gene Panels: Sequence specific genes or regions of interest, commonly used in cancer genomics.

- Metagenomics: Analyze microbial communities by sequencing 16S rRNA genes or whole genomes.

- Small Genome Sequencing: Perfect for sequencing viral, bacterial, or other small genomes.

 

 

3. Oxford Nanopore Technology (ONT) Service

 

• Overview:

Our Oxford Nanopore Technology service offers real-time, long-read sequencing, allowing for detailed analysis of complex genomic regions. ONT's flexibility and portability make it a powerful tool for a wide range of sequencing applications.

 

• Advantages:

- Long Reads: Capable of sequencing reads over 100,000 base pairs, enabling the analysis of complex regions such as structural variants and repetitive sequences.

- Real-Time Data: Immediate analysis as sequencing occurs, providing instant insights.

- Portability: ONT devices are portable, making them ideal for field sequencing and remote applications.

 

• Applications:

- Structural Variant Detection: Identify large insertions, deletions, and other structural variations with high accuracy.

- Transcriptomics: Sequence full-length RNA molecules to study transcript isoforms, gene fusions, and alternative splicing.

- De Novo Genome Assembly: Assemble genomes from scratch, particularly useful for complex or repetitive sequences.

- Field Sequencing: Perform sequencing in remote or on-site locations, ideal for environmental studies and epidemiology.

 

4. Sanger Sequencing Service

 

• Overview:

Our Sanger Sequencing service provides the gold standard for DNA sequencing, offering unmatched accuracy and reliability. It is particularly well-suited for smaller-scale projects or applications where precision is critical.

 

• Advantages:

- High Accuracy: Ideal for validating genetic variations and confirming results from high-throughput sequencing.

- Long Read Lengths: Generates reads up to 1000 base pairs, perfect for sequencing specific genes or regions.

- Targeted Applications: Best for mutation detection, validation studies, and small-scale sequencing projects.

 

• Applications:

- Mutation Detection: Identify single nucleotide polymorphisms (SNPs) and small insertions/deletions in specific genes.

- Validation: Confirm high-throughput sequencing results in clinical and research settings.

- Targeted Gene Sequencing: Sequence individual genes, plasmids, or small DNA fragments with precision.

 

 

Why Choose GENXMAP?

 

At GENXMAP, we are committed to delivering high-quality sequencing services that meet the specific needs of your research or clinical project. Our advanced technologies and expert team ensure that you receive accurate, timely, and cost-effective solutions for all your sequencing needs. Whether you are conducting targeted gene studies, large-scale genomic research, or exploring new frontiers with long-read sequencing, GENXMAP provides the tools and expertise to support your success.

 

 

Contact us today to discuss how our sequencing services can advance your research. Let us help you unlock the full potential of your genomic discoveries.