I have a collaborator who amplified V3 regions using the following primers:
Forward
aatgatacggcgaccaccgagatctacactctttccctacacgacgctcttccgatctNNNNCCTACGGGAGGCAGCAG
Reverse (one of 10)
caagcagaagacggcatacgagatgtgactggagttcagacgtgtgctcttccgatctACATCGATTACCGCGGCTGCTGG
Italics are flow cell adapter sequence, underline is Illumina sequencing primer site, bold caps is index sequence, and plain caps is V3 primer. I know the index site is not where Illumina usually puts it (these are downstream of the sequencing primer, Illumina puts them upstream of the sequencing primer), but he swears he used these before with the index site moved like this and it worked.
The indexes used do not match normal "TruSeq" indexes, but they do match the TruSeq Small RNA primers (RPI1, RPI2, etc.).
My questions:
1. Can the MiSeq read the indexes and demultiplex if the indexes are moved?
2. If the indexes can be read, can I run these samples as "Small RNA" instead of "TruSeq" on the MiSeq so I can plug in the matching index IDs? Or do I leave the demultiplexing up to my collaborator who says he had to do it before anyway so can do it again.
3. The sequencing primer site for "Small RNA" is different than the sequencing primer site for "TruSeq"? Will this confuse the sequencer?
Thank you for your input!
Forward
aatgatacggcgaccaccgagatctacactctttccctacacgacgctcttccgatctNNNNCCTACGGGAGGCAGCAG
Reverse (one of 10)
caagcagaagacggcatacgagatgtgactggagttcagacgtgtgctcttccgatctACATCGATTACCGCGGCTGCTGG
Italics are flow cell adapter sequence, underline is Illumina sequencing primer site, bold caps is index sequence, and plain caps is V3 primer. I know the index site is not where Illumina usually puts it (these are downstream of the sequencing primer, Illumina puts them upstream of the sequencing primer), but he swears he used these before with the index site moved like this and it worked.
The indexes used do not match normal "TruSeq" indexes, but they do match the TruSeq Small RNA primers (RPI1, RPI2, etc.).
My questions:
1. Can the MiSeq read the indexes and demultiplex if the indexes are moved?
2. If the indexes can be read, can I run these samples as "Small RNA" instead of "TruSeq" on the MiSeq so I can plug in the matching index IDs? Or do I leave the demultiplexing up to my collaborator who says he had to do it before anyway so can do it again.
3. The sequencing primer site for "Small RNA" is different than the sequencing primer site for "TruSeq"? Will this confuse the sequencer?
Thank you for your input!
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