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5. Sequencing run
  • Introduction
  • 1. Software installation
  • 2. Hardware check
  • 3. Flow cell check
  • 4. Library preparation
  • 5. Sequencing run
  • 6. Results and metrics
  • 7. Next steps
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You are in the ‘Linux’ branch of Software installation.
Change branch:
5.7

Launch EPI2ME and start workflow

Need help?

Now your sequencing run is started, it is a good time to get EPI2ME running in the background. This allows reads to be sent into the workflow as soon as they have been acquired and basecalled.

If you have closed the EPI2ME Agent from earlier, please reopen it:

Agent icon

Click New analysis and select FASTQ control experiment.

Homepage new analysis

Analysis control experiment DNA

If prompted, select a folder containing FASTQ files to be analysed. If a MinKNOW-generated folder structure is detected in the default input location, this will be shown in the Experiments & samples tab. You can change the default input location in the Settings page (cog icon) under Data sources.

Settings icon

Alternatively, you will be directed to the Folders tab, where you can select your input folder.

Select folder

Adjust the run-time parameters of your analysis:
Select No under "Are you uploading human DNA/RNA?". Leave all the other settings at their default values, then click Accept & Start.

Screenshot 2021-02-09 at 15.18.33

EPI2ME will start the workflow.

Analysis in progress Control DNA

EPI2ME workflow now running

The EPI2ME workflow is now running. You can minimize the client window and let it run in the background.

Prev 6. Results and metrics

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