So we don't need to buy it from Illumina, right? Can I design it and synthesize from routine nuclear acid primer company? will this cheaper than Illumina? What's the cost for 2048 barcodes? Thanks.
Hello. I want to run around 50 samples on a HiSeq lane. I have done this on MiSeq with success and am just scaling up. With the MiSeq I ran 11 samples with 11 barcodes as that's all I was given (they are custom primers). So now I need more barcodes (6 nucleotides). I'm sure I could generate a load of random barcodes but I want to make sure they don't cause havoc. Is there a best practise for barcode generation in this situation?
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Index design and analysis software for Meyer M, Kircher M. Illumina sequencing library preparation for highly multiplexed target capture and sequencing. Cold Spring Harb Protoc. 2010 Jun 1;2010(6) doi:pdb.prot5448. PubMed PMID: 20516186
https://bioinf.eva.mpg.de/multiplex/
- Designing index sequences with some edit distance (create_index_sequences.py)
- Selecting a balanced subset of indexes (suggest_subset.py)
- Evaluating the channel/base composition of a defined set of indexes (eval_selection.py)
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Are you familiar with dual-indexing?
No. But I guess what I'm asking is whether I can use a load of made up barcodes for single indexing or how I minimise confusion between barcodes when sequencing