R&D
Expert guidance for transcriptomic discovery and assistance in setting up your experiment with professional precision.
UNLOCKING CELLULAR INSIGHTS WITH TRANSCRIPTOMIC SEQUENCING SERVICES
At Amplexa we specialize in offering comprehensive solutions for transcriptomic explorations and discoveries. Amplexa has experience from various field of science, techniques, and bioinformatic approaches for unraveling the transcriptomic profile of biological samples, both in bulk and at a single-cell level. We offer both the complete solutions, and collaborative projects.
BULK RNA SEQUENCING
WHY CHOOSE BULK RNA SEQUENCING?
Bulk RNA sequencing is a powerful technique for uncovering the transcriptional profile of a pool of cells.
Whether you are interested in discovering the transcriptional consequence of your loss-of-function experiment, or identifying the transcriptional regulators that are differential for persistor cells in your bacterial strain, bulk RNA sequencing will be a technique that delivers high resolution data and easy interpretable results (17).
We recommend selecting bulk RNA sequencing for direct comparisons between two or more conditions, as it effectively captures the total transcriptomic differences between groups, providing valuable insights into the conditional variations.
BULK RNA SEQUENCING
- I am a researcher: I need to discover the transcriptional landscape of a relatively homogeneous sample.
Technique description: Bulk RNA sequencing is useful for the identification of transcripts in an isolated sample. Bulk RNA-seq offers in-depth discoveries of differentially expressed genes between two or more conditions.
SINGLE CELL SEQUENCING
WHY CHOOSE SINGLE CELL SEQUENCING?
Single cell sequencing has the potential to unravel heterogeneous molecular mechanisms otherwise unnoticed, that is characteristic for pathogenesis of disease, by measuring the transcript levels in thousands of cells, simultaneously (16).
Amplexa has in-house solutions for both library preparation through 10X-Genomics platform, and bioinformatic expertise for analysis and interpretation.
We recommend selecting single cell sequencing when knowledge on non-homogenous cell populations is central, as the technique will widen the resolution, and enhance the interpreted outcomes.
SINGLE CELL SEQUENCING
- I am a researcher: I need to identify specific cell types and subpopulations in a sample.
Technique description: Single cell techniques are methods for analyzing the expression profile at a single cell resolution rather than mixing all cell types as in bulk assays.
BIOINFORMATICS
Bioinformatics has helped clients advance their research in various fields, including microbiology and basic research on stem cell regeneration.
We offer a complete package, from helping you set up your experiment to unlock the full potential to interpreting the analyzed results and generating publishable figures. We also acknowledge researchers' wish to make their own interpretations of the data and therefore offer a fast and easy solution for secure data transfer.
BIOINFORMATICS
- I am a researcher: I need data analysis and interpretation for my findings.
Technique description: Amplexa Genetics will organize the new data and combine it with databases and, through statistics, will designate important parts that can be used to draw conclusions within diagnosis and research.