Hello community,
we have a problem concernig a illumina sequenced ChIPSeq experiment.
After mapping and viewing the reads in the UCSC GB surprisedly 99% of the reads map to some unique locations. The corresonding reads share the same start and end coordinate and there are no additional cluster of duplication surrounding a location in terms of the origional fragment lenght.
Does anyone have an idea? I would very much appreciate your assistance
tec
we have a problem concernig a illumina sequenced ChIPSeq experiment.
After mapping and viewing the reads in the UCSC GB surprisedly 99% of the reads map to some unique locations. The corresonding reads share the same start and end coordinate and there are no additional cluster of duplication surrounding a location in terms of the origional fragment lenght.
Does anyone have an idea? I would very much appreciate your assistance
tec
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