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Old 09-12-2018, 06:09 PM   #1
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Location: vietnam

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Default How to fix the Gen sequence

How to fix the Gen sequence
* I wonder what is the biggest difference between demonstrating a sequential profile of the next Gen sequence versus making a profile through SAGE with the classic Sanger sequence?
Specifically I want to clarify the number
Thank you
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Old 09-12-2018, 08:03 PM   #2
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RNA-Seq may use 10-30 million reads in an experiment for expression profiling. SAGE would collect 10-50 thousand SAGE tags or so for a profile?
Providing nextRAD genotyping and PacBio sequencing services.
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