FAQs
- What are the DNA and Protein Index sequences?
- What sequencing coverage is recommended?
- Can I pool and sequence DNA and protein libraries simultaneously?
- What if my pass-filter read is < 85 % after sequencing?
- Are Custom Sequencing Primers required?
- What causes a low % of mapped reads to cells?
- Which sequencing chemistry do you recommend?
- What loading concentration should I use?
- What concentration of PhiX should I use?
- Can I pool Tapestri and other libraries on my sequencer?
- Can I use PE 250 bp sequencing chemistry to improve FLT3-ITD detection?