Perform QIAseq UPXome RNA Expression and Fusion Calling (N6-T RT + ODT-RT primer)

The Perform QIAseq UPXome RNA Expression and Fusion Calling (N6-T RT + ODT-RT primer) template workflow supports a combined N6-T RT primer + ODT-RT primer protocol. All reads are used for gene expression analysis while the reads amplified by the N6-T RT primer are used for studying transcript expression and fusions.

The Perform QIAseq UPXome RNA Expression and Fusion Calling (N6-T RT + ODT-RT primer) workflow can be found here:

        Template Workflows | Biomedical Workflows (Image biomedical_twf_folder_open_16_n_p) | QIAseq Sample Analysis (Image qiaseqrna_folder_closed_16_n_p) | QIAseq RNA Workflows (Image qiaseq_workflows_folder_closed_16_n_p) | Perform QIAseq UPXome RNA Expression and Fusion Calling (N6-T RT + ODT-RT primer) (Image quantify_qiaseq_upx_16_n_p)

Or run directly from the Analyze QIAseq Samples guide:

        Template Workflows | Biomedical Workflows (Image biomedical_twf_folder_open_16_n_p) | QIAseq Sample Analysis (Image qiaseqrna_folder_closed_16_n_p) | Analyze QIAseq Samples (Image qiaseq_panel_guide_16_h_p)

where it is available in the the UPXome RNA tab, under QIAseq UPXome Library Kit, and setting analysis to N6-T RT primer + ODT-RT primer.

The workflow is identical to the Perform QIAseq FastSelect RNA Expression and Fusion Calling (N6-T RT + ODT-RT primer) workflow described in Perform QIAseq FastSelect RNA Expression and Fusion Calling (N6-T RT + ODT-RT primer) The only difference being that the Perform QIAseq UPXome RNA Expression and Fusion Calling (N6-T RT + ODT-RT primer) workflow starts by demultiplexing the input into samples that correspond to plate wells.

The workflow is run as described in Running the QIAseq UPXome workflows.



Subsections