I am wondering why some Illumina platform (e.g. HiSeq) allow for sequencing of libraries with no index reads, while others do not (e.g. NovaSeq and MiSeq)? Are index reads used for cluster identification in the latter case?
Thank you for your answer. I am asking because I have in-line barcodes in my Illumina libraries that are sequenced by an external company on HiSeq. Due to discontinuation of HiSeq, the company urged me to include standard indexes in the design but I cannot quite understand why in-line barcodes would not be compatible with other sequencing platforms, like NovaSeq.