Whole RNA Sequencing

Dive into the world of RNA sequencing with our customized Whole Transcriptome Sequencing services. We don’t just provide raw sequencing data; we deliver a tailored analysis to streamline your research focus. Our services encompass differential gene expression, novel transcript identification, and splice variant analysis, among others, all designed to meet your specific research objectives. With our expert analysis, you gain insights into the complex world of RNA, propelling your innovative research to new heights.


Additional benefits:


3-year warranty and safe storage of data with unlimited access: The generation of sequencing data can lead to large and complex data sets, demanding significant storage space that may not be readily available or cost-effective for individual researchers or smaller institutions. By storing raw and analyzed data on our secure servers, we relieve you of the burden of data management. Additionally, the three-year unlimited access allows you to revisit and analyze the data for new insights as your research evolves, which is particularly valuable for long-term projects and follow-up studies.


24-hour response time: By providing timely responses, we ensure that these crucial insights aren't lost or delayed, allowing for the necessary adjustments to the analysis or experiment design to be made swiftly. This quick feedback loop aids you in keeping your project on track, enhances the iterative process of scientific inquiry, and ultimately contributes to more robust and insightful outcomes. With us, your questions are promptly addressed, keeping your research moving forward without delay.


Hard to process sample preparation: Nucleic acid isolation can be a challenging process, especially from difficult-to-process samples such as formalin-fixed, paraffin-embedded (FFPE) sections. For many researchers, especially those without access to specialized lab equipment or expertise, this can be a significant hurdle. However, with our service, we eliminate this concern. We handle the complex process of nucleic acid isolation from any sample you provide, ensuring that even the most challenging materials are effectively processed.


Ready to use full materials and methods and publication data: Providing a ready-to-use, comprehensive materials and methods and descriptions is a key component of our service. Drafting a materials and methods section can be time-consuming and complex, potentially requiring several hours to days of a researcher's time depending on the complexity of the procedures used. By supplying a detailed, publication-ready description, we free up significant time for our customers.

Information requested when ordering a product:



Examples Of What You Can Do

By contrasting gene expression between distinct samples, scientists can discover patterns and variances in gene regulation potentially associated with specific conditions or diseases. RNA sequencing, for instance, can be employed to compare gene expression in healthy individuals versus those afflicted by a particular disease, assisting in the identification of genetic factors linked to the disease.


In addition, RNA sequencing can be utilized to compare gene expression in different cell lines, model organisms, or individuals before and after a specific drug treatment, revealing potential therapy targets or biomarkers of treatment response. Within the field of cancer research, RNA sequencing proves beneficial for contrasting the gene expression of diverse tissues or cell types, thereby enhancing our understanding of mechanisms underlying normal physiology or disease processes.


Moreover, exploring gene expression differences can validate experimental findings and furnish critical data to support scientific publications. By scrutinizing gene expression differences in numerous samples, researchers can bolster the robustness of their findings and provide more comprehensive evidence to substantiate their research conclusions.

RNA sequencing provides simultaneous analysis of thousands of genes’ expression levels, granting a more comprehensive understanding of the biological processes impacted by a drug. By comparing pre and post-drug treatment gene expression profiles of cells or tissues, researchers can pinpoint specific pathways and genes influenced by the drug.


This critical information can evaluate a drug’s potential efficacy and safety, and identify valuable biomarkers for patient selection or monitoring treatment response. RNA sequencing proves to be an essential tool in expediting drug development and enhancing patient outcomes.

RNA sequencing facilitates the detection of a broad spectrum of pathogens, including viruses, bacteria, and fungi, through the analysis of the pathogen’s genetic material. This methodology delivers a comprehensive understanding of the pathogen and its virulence factors, informing the development of effective treatment and control strategies.


Furthermore, RNA sequencing can examine the host response to the pathogen, assisting in the identification of potential therapeutic targets or disease severity biomarkers. By offering a more in-depth insight into the pathogen, RNA sequencing enhances diagnostic accuracy and speed. It also provides valuable data for public health initiatives to prevent the spread of infectious diseases.


RNA sequencing enables the identification of genes and pathways associated with particular traits or phenotypes, thereby enriching our comprehension of the biological mechanisms underlying these traits. This technique offers critical insights into the genetic basis of complex traits such as disease susceptibility or drug response, assisting in the identification of potential therapeutic targets.


Utilizing RNA sequencing to support phenotypic discovery can furnish invaluable data for scientific publications, enhancing the impact and visibility of your research. At Deep Biotech Solutions, we employ advanced RNA sequencing methods to expedite your phenotypic discovery research, enhancing your project’s reach and influence in the scientific community. Capitalize on our state-of-the-art RNA sequencing services to drive your phenotypic discovery forward.

Frequently Asked Questions

Whole RNA Sequencing, or transcriptome sequencing, is a technique that allows us to study the complete set of RNA transcripts produced by the genome. It can help identify differentially expressed genes, novel transcripts, and splice variants, providing insights into gene function and regulation.

Our Whole RNA Sequencing service uses advanced bioinformatics tools to analyze differential gene expression, allowing us to identify which genes are up- or down-regulated under specific conditions. This information can be crucial for understanding disease mechanisms or responses to treatments.

Your raw and analyzed data will be safely stored on our secure servers with unlimited access for three years. This means you can access and analyze your data whenever you need, which is particularly useful for long-term research projects and follow-up studies.

Our service is equipped to handle nucleic acid isolation from any sample type, including those that are difficult to process such as formalin-fixed, paraffin-embedded (FFPE) sections. Our specialized techniques ensure high-quality results regardless of sample complexity.

Our Whole RNA Sequencing service is capable of identifying novel RNA transcripts that may not be annotated in existing databases. This can reveal new aspects of gene regulation and function, and can be particularly valuable in exploring uncharted areas of genomics.

Splice variant analysis can provide insights into alternative splicing events, which can result in different protein products from the same gene. Understanding these variations can give valuable information about gene regulation, function, and its potential role in diseases.

Our 24-hour response time means we will respond to any questions or requests related to your RNA sequencing project within a day. This allows for timely adjustments to be made to the analysis or experimental design, keeping your project on track and facilitating more robust and insightful outcomes.

We use Artificial Intelligence to handle the vast data generated by Whole RNA Sequencing. AI can help identify patterns and make predictions that may not be possible with traditional data analysis methods, providing deeper and more meaningful insights into your transcriptome data.

Yes, our Whole RNA Sequencing service is capable of identifying and analyzing both coding and non-coding RNAs, including microRNAs, long non-coding RNAs, and circular RNAs, which can provide additional layers of gene regulatory information.

This service provides a detailed, publication-ready materials and methods section, saving you significant time and effort in preparing this complex part of a research manuscript. The provision includes all methods related to the RNA sequencing process and subsequent bioinformatics analyses.

Reach out to us if you have any queries about our products. We assure you of a response within 24 hours.

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