Hi,
We performed a full plate amplicon run on 454 FLX, on a gene library in which a single mutation was introduced to each molecule at a different position. We are observing a ~5X higher mutation rate in the 454 library reads compared to the mutation rate observed in Sanger sequencing of variants, and higher than could be explained due to sequencing errors.
We are thinking this may be due so-called "PCR Jumping" during the amplicon PCRs in which incomplete products can hybridize to other templates and end up with hybrid products with multiple mutations. Has anyone seen this in their amplicon runs, or have any thoughts about how to reduce this?
Thanks,
Elad
We performed a full plate amplicon run on 454 FLX, on a gene library in which a single mutation was introduced to each molecule at a different position. We are observing a ~5X higher mutation rate in the 454 library reads compared to the mutation rate observed in Sanger sequencing of variants, and higher than could be explained due to sequencing errors.
We are thinking this may be due so-called "PCR Jumping" during the amplicon PCRs in which incomplete products can hybridize to other templates and end up with hybrid products with multiple mutations. Has anyone seen this in their amplicon runs, or have any thoughts about how to reduce this?
Thanks,
Elad
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