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03-16-2017, 07:16 PM
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Junior Member
Location: Singapore Join Date: Mar 2017
Posts: 1
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NoME-seq question
Hello SeqAnswers community ,
I am new to NoME-seq and I have a few questions. Firstly, is there any advantage of going with paired end read versus single end reads, and second, what is a good starting total reads required i.e 100,200 300 million ? We are interested in mapping nucleosome occupancy differences at repetitive elements between treatment and control groups. Thanks! Dennis |
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