Hello,
I just got my Solexa data. I got the FastaQ files. Since this is my first time, I have some questions:
1. What can be done to assure the quality of the sequences.?
2. I obtained ~6 million reads per library, does this sound normal?
3. How to convert Illumina quality scores to Phd scores?
4. what is the best algorithm for de novo assembly.
I appreciate any help
I just got my Solexa data. I got the FastaQ files. Since this is my first time, I have some questions:
1. What can be done to assure the quality of the sequences.?
2. I obtained ~6 million reads per library, does this sound normal?
3. How to convert Illumina quality scores to Phd scores?
4. what is the best algorithm for de novo assembly.
I appreciate any help