Reprever

Reprever: resolving low-copy duplicated sequences using template drive

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Last Update: 2015-12-03

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For any genomic regions that are increased in copy number, Reprever identifies:

(a) the insertion breakpoints where the extra duplicons inserted into the donor genome

and

(b) the actual sequence of the duplicon

For more details, please refer to our paper in Nucleic Acids Research http://nar.oxfordjournals.org/content/41/12/e128.long

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2013-07-23

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$300 Free Credits to Build on Google Cloud

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Put your $300 in credit toward real workloads, then keep building with free monthly usage for 20+ products. No commitment and no charge until you upgrade.

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