What is nucleotide diversity and why is it important? Adapter dimers: causes, effects, and how to remove them Does my sequencing run look good?
Sequencing Method Explorer: Which NGS method is most suitable for my research? System checks for Illumina sequencing platforms What is the PhiX Control v3 Library and what is its function in Illumina Next Generation Sequencing? PhiX loading concentrations for validation runs on Illumina sequencing platforms What is the final formamide concentration in the waste solution of Illumina sequencing systems? How much PhiX spike-in is recommended when sequencing low diversity libraries on Illumina platforms? Why sequencing 26 or more cycles in Read 1 is recommended How many cycles of SBS chemistry are in my kit? How short inserts affect sequencing performance Is it possible to pool different library types in the same sequencing run? Considerations when migrating non-Illumina libraries between sequencing platforms