Is it possible to re-amplify the cDNA in case it is low yield? Read answer: Is it possible to re-amplify the cDNA in case it is low yield?
Can we use less than 10ng cDNA for library preparation? Read answer: Can we use less than 10ng cDNA for library preparation?
What does it mean if I see an unexpected fragment profile, or unexpected peaks (e.g., primer dimers, RBC, etc.)? Read answer: What does it mean if I see an unexpected fragment profile, or unexpected peaks (e.g., primer dimers, RBC, etc.)?