At Biogenity, we offer complete transcriptomics workflows, covering everything from sample preparation to data analysis. We analyze the expression of RNA with a focus on quality and interpretability to ensure ready-to-use material for internal documentation, publications, or presentations.
Transcriptomics is the study of Ribonucleic acids (RNA) and provides crucial insight into the functional genome, which can provide the foundation for understanding biological mechanisms and states. Whether investigating mRNA, microRNAs, or other small RNAs, RNA serves as critical information when investigating biological systems. Multiple transcripts and their expressions can be analyzed using modern high-throughout methods to assess different pathological or physiological conditions, e.g., studying drug mode of action or characterizing molecular signatures for biomarker discovery.
If you’d like to learn more, we are happy to discuss your project and help you get the most out of your peptide analysis.
Illumina NGS
HiSeq, NextSeq and NovaSeq
< 500 pg RNA
very low inputs detected
mRNA, microRNA, small RNA
from cells, tissue, EVs, biofluids
At Biogenity, we understand that transcriptomics research is a sophisticated field that demands precision, expertise, and a tailored approach. Our team of transcriptomics experts is dedicated to guiding you through every step of your study, ensuring your project not only succeeds but also contributes to your scientific venture.
We invite you to an online consultation, during which we can address your questions and offer an expert assessment of how our transcriptomics strategies can be customized to meet your research goals.
At Biogenity, we pride ourselves on our customized approach to transcriptomics sample preparation, backed by a team of experienced professionals and specialized partners. Understanding that each research aim is unique, we will discuss the most suitable workflows for your study.
We can work with various transcriptome samples, including biofluids, cells, extracellular vesicles, and tissue. Our commitment to quality and care ensures that whether you require partial or complete sample preparation, your samples receive the expert handling they deserve. With Biogenity, rest assured that you're equipped with the best approach for your research.
We pride ourselves on being able to offer various innovative Next-Generation Sequencing (NGS) platforms. We have a wide range of Illumina instruments available, including the HiSeq for high-complexity analysis, NextSeq for smaller studies, and the ultra-fast and high-performing NovaSeq.
High sensitivity or selectivity may be the key to answering your research questions, depending on the research objective. Biogenity offers high-throughput transcriptome solutions to analyze entire transcriptomes, and also investigate specific gene expressions. We can detect very low RNA inputs from various cells and tissues down to < 500 pg.
At Biogenity, we can perform the data analysis for you, allowing you to spend more time understanding the biology in your transcriptomics samples. Our team consists of experts in statistics and bioinformatics that do everything from filtering to generating diagnostic models.
Biogenity allows you to integrate different data sources to answer your research questions. Suppose you want to combine omics data or use clinical data to expand the analysis of your samples. In that case, we can assist you with the data analysis to do multiomics or machine learning studies using your data. Contact us today, and let's explore the opportunities to integrate additional data in your research.
At the conclusion of our transcriptomics analysis, we ensure a seamless transition from discovery to application. We deliver detailed reports and data, followed by a post-delivery consultation to discuss your study's insights and findings.
What to expect during post-consultation:
Together, we ensure that you have the best prerequisite for your further research. The consultation can also be used to explore the next step, whether you are looking to expand the project with additional omics studies or validate the results.