Hi everybody,
to prepare the 8 kb PE library the DNA have to be fragmented to 8 kb of size using the hydroshear, I know this is a critical step.
Do you have suggestion or tips to do this?
Does anyone tried an alternative method to obtain the fragments in the right size range?
Thanks,
bia
to prepare the 8 kb PE library the DNA have to be fragmented to 8 kb of size using the hydroshear, I know this is a critical step.
Do you have suggestion or tips to do this?
Does anyone tried an alternative method to obtain the fragments in the right size range?
Thanks,
bia
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