Troubleshooting and FAQs
The most commonly asked questions
- What do large DNA fragment sizes in Bioanalyzer/TapeStation mean?
- My library is enriched for fragments at ~125-150 bp. What does this mean?
- What do adapter dimers look like in CUT&RUN and how do I avoid them?
- When should I remove adapter dimers? What protocol do you recommend?
- Do I need to sequence an input control?
- Why is there background in open chromatin in my sequencing data?
- Why is there high background in my sequencing data?
- How many reads do I need for E. coli Spike-in DNA and the K-MetStat Panel?