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Old 03-16-2017, 08:16 PM   #1
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Location: Singapore

Join Date: Mar 2017
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Default 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!

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