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  • flobpf
    Member
    • Apr 2010
    • 76

    #1

    RAD-seq adapter design

    Hi

    I was planning a RAD-seq experiment for about 90 ecotypes. The costs of ordering 180+ HPLC purified and modified oligos for those many samples are quite prohibitive. Hence, I was thinking of a double-index strategy for pooling all my samples using Illumina, and I wonder if someone could provide some feedback on whether the following oligo design would be appropriate for Illumina and RAD-seq.

    So essentially, the P1 adapter would be

    Code:
    Read 1 sequencing primer -- Barcode -- REoverhang
    
    ACACTCTTTCCCTACACGACGCTCTTCCGATCT -- AACTA -- CAT*G
    The P2 adapter would be

    Code:
    Read 2 sequencing primer -- IlluminaIndex -- P7 attachment site
    so that the final DNA would look like:

    Read 1 sequencing primer -- Barcode -- REoverhang --DNA of interest --Read 2 sequencing primer -- IlluminaIndex -- P7 attachment site
    I would also have to order two primer oligos for PCR amplification:
    Code:
    P5 attachment site -- Read1 SeqPrimer --> 1 primer
    P7 attachment site -- IlluminaIndex -- Read2 SeqPrimer --> 10 primers
    based on the information provided here

    Thus, if I do Paired End sequencing, then for 90 ecotypes, I calculated that I would just need to order
    P1: 10*2 = 20 (*2 to make double strand)
    P2: 10*2 = 20
    PCR primers: 11
    Total=51
    instead of ~200 odd oligos for the regular RAD-seq protocol, leading to significant cost savings. One drawback is that I won't be able to pool the samples after attaching the P1 adapter; instead I can only pool in sets of 10. However, given the cost savings, I think that is ok.

    Does this strategy sound feasible?
    Last edited by flobpf; 06-02-2014, 09:08 AM.

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