A powerful technique for uncovering the transcriptional profile of a pool of cells.
To unravel various biological systems, it is essential to understand the complexity of transcriptomic changes. Bulk RNA sequencing serves to obtain a high-throughput representation of average transcriptomic changes between two or more conditions. Depending on the type of samples, you can use bulk RNA sequencing in:
Sample type: BACTERIA
Sample type: HUMAN BIOPSIES and ANIMAL MODELS
When investigating splice variants, sequencing deeper is typically recommended(8). In principle, we can sequence as deep as necessary, and this will be a topic that is always discussed in the introduction consultation.
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.
To help ensure more accurate results before sending samples to Amplexa Genetics, you should meet certain quality measures