GENXMAP offers a comprehensive range of cutting-edge sequencing services tailored to the diverse needs of research and clinical applications. We provide Sanger sequencing solutions for targeted studies and next-generation sequencing (NGS) using platforms such as NovaSeq 6000, MiSeq, MGI, and Oxford Nanopore Technologies (ONT). Each technology is optimized for specific applications, from large-scale projects like whole-genome studies to targeted analyses such as transcriptome sequencing. These platforms ensure exceptional coverage, depth, and accuracy, enabling the discovery of crucial genetic insights, whether rare variants or complex gene expression profiles.
We provide personalized support at every stage of your project. From defining scientific objectives to sample preparation, bioinformatics analysis, and result interpretation, our team of experts guides you to obtain relevant and actionable results. We place a strong emphasis on data quality and ensure seamless communication with our clients throughout the process, guaranteeing that your specific needs are always considered and that results are delivered on time.
Pure RNA, Unlocking Precision Analysis
Optimized and Transparent Services
Our Go/No-Go processes allow you to track the progress of your project in real-time. At each stage, you validate the transition to the next, ensuring complete control and maximum transparency throughout the entire process.
Our optimized timelines ensure fast and efficient execution of each project while meeting your specific requirements. This system ensures proactive time management, minimizing delays and maximizing productivity to deliver results that align with your expectations.
Our tailored processes are designed to meet the unique needs of each project, offering flexibility and personalized follow-up. This system ensures rigorous control while delivering accurate results that align with your expectations.
Our detailed analyses guarantee reliable and in-depth results tailored to each study. With cutting-edge tools and proven methodologies, we provide a precise understanding of genetic data, while adhering to the highest standards of quality and scientific rigor.
GENXMAP, your trusted partner to support you in your research.
Precision and Versatility for All Applications
We offer precise and versatile RNA sequencing services, tailored to your specific needs, using advanced technologies for accurate, fast, and cost-effective solutions.
Sanger Sequencing
Sanger sequencing provides top-tier accuracy and reliability, making it ideal for small-scale projects or critical validations.
Advantages:
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High precision, long reads, and optimal performance for targeted projects.
Applications:
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Mutation detection, sequencing validation, and targeted gene sequencing.
MiSeq
Perfect for projects requiring fast and accurate results on a small scale, the MiSeq is ideal for targeted sequencing and small genomes.
Advantages:
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Fast turnaround time, versatility for various applications, and high-quality data.
Applications:
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Targeted gene panels, metagenomics, and small genome sequencing.
NovaSeq 6000
Providing unmatched power for complex genomic projects, the NovaSeq 6000 is ideal for large-scale and high-resolution sequencing.
Advantages:
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Exceptional scalability, flexibility for various projects, and cost-efficiency for large-scale analyses.
Applications:
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Whole genome sequencing, exome sequencing, and large-scale transcriptomics, including single-cell RNA-Seq.
Oxford Nanopore Technology (ONT)
ONT sequencing directly analyzes native DNA and RNA, providing long reads and real-time detection of post-transcriptional modifications.
Advantages:
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High accuracy, long reads, detection of splicing variants, and instant analysis.
Applications:
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Native RNA studies, whole genome sequencing, and biomedical research.
Discover Our Blog
Precision, Innovation, and Reliability at the Service of Your Discoveries.
Explore our blog to learn how our cutting-edge technologies and advanced analyses are opening new perspectives in scientific research and clinical applications.
Service Details
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We clearly define your scientific objectives to guide your study, whether it's analyzing specific markers via RT-qPCR or exploring further with analyses such as Bulk RNA-seq or single-cell RNA-seq. Each approach is tailored to your needs to maximize the relevance and precision of the results.
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You specify the types of samples you wish to analyze (tissues, cells, environmental samples, etc.), allowing us to adapt the extraction process to ensure the quality and accuracy of the results.
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Methodology Selection:
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Based on your objectives, we provide guidance on the most suitable method for your analysis.
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Sequencing Platform Selection:
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We discuss the available options based on sample complexity and the required resolution (Illumina, MiSeq, Oxford Nanopore Technology).
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Budget and Timeline Estimation:
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Budget Validation: We provide a clear estimate of the project cost based on the chosen methodology, the number of samples, required coverage, and additional bioinformatics analyses.
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Timeline Planning: We share an estimated timeline for sample preparation, sequencing, and bioinformatics analysis, with regular checkpoints to track progress.
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Continuous Monitoring and Support:
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Ongoing Support: Once the project is launched, we support you throughout the entire process, from raw data collection to bioinformatics assistance for result interpretation, providing personalized reports and recommendations for next steps.
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GENXMAP utilizes the following advanced sequencing platforms:
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NovaSeq (Illumina)
Advantages:
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Rapid and accurate sequencing of large DNA quantities from diverse environmental or biological sources.
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High coverage and depth, enabling precise detection of microorganisms present in samples.
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MiSeq (Illumina)
Advantages:
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High precision: Illumina's sequencing-by-synthesis technology is renowned for its low error rate, ideal for high-precision analyses, such as genetic variation studies.
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Quick turnaround: Short run times allow for timely results, ideal for urgent projects.
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Oxford Nanopore Technology (ONT)
Advantages:
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Long reads: ONT enables the generation of long reads (up to several hundred kb), making it invaluable for studying complex genomic regions, entire genomes, and full-length transcripts without fragmentation.
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Real-time data: Immediate analysis as sequencing occurs, providing instant insights.
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Step 0 >> Sample Reception Control
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Visual evaluation for quantity and quality.
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Report and client decision "Go / No-Go" for the continuation of the process.
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Step 1 >> Sample Preparation
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Acceptance of various sample types:
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Purified RNA (ideally >50 ng/µL).
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Tissues, cells, or biological fluids for extraction by GENXMAP.
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Sample quality control:
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Measurement of concentration (Qubit, NanoDrop).
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Integrity assessment via electrophoresis or Bioanalyzer.
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Step 2 >> Library Preparation
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Adaptation of preparation based on:
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Type of sample (genomic DNA, plasmids, PCR, etc.).
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Project objective (targeting, exome, transcriptome).
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Customization options for specific needs.
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Step 3 >> Sequencing
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Execution on the selected NGS platform.
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Adjustment of sequencing depth to meet coverage and sensitivity requirements.
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Step 4 >> Bioinformatics Analysis
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Various types of analyses are possible depending on the project (Bulk, scRNA-seq, or spatial transcriptomics).
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Step 5 >> Delivery of Results
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Results provided (FASTQ + bioinformatics analysis reports if the option is chosen) via a secure platform or external storage disk.
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Technical support for data interpretation and utilization.
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Bulk RNA-seq
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scRNA-seq
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Transcriptomique spatiale
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