Hello everyone, I request you all to kindly help me by answering the following questions:
Would be very helpful if you do so.
- How to select the threshold for the base quality parameters while processing the NGS reads till finding variants?
- Difference between V3-V4 and V4 amplicon sequencing and its applications. Which one of the techniques can detect a large set of organisms?
- Can you please explain the quality filters that can be used for processing microarray data in genome studio?
Thanking you in anticipation.