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written 17 months ago by
shenwei356 ♦ 4.1k
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Istvan Albert ♦♦ 77k
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QVINTVS_FABIVS_MAXIMVS • 2.1k
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Neilfws ♦ 48k
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C: Efficiently aligning a lot of reads on the same small reference sequence by
cedric.stroobandt • 0
The data is indeed fastq format. I was mainly wondering if there existed specific alignment meth...
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I must have misunderstood at some point, I though you were interested in CD40 status. Yes, if you...
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The sign in PCA is arbitrary, you'll get opposite signs randomly depending on how exactly the PCA...
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The only commonly used tool like this is Galaxy, for which you simply write an XML wrapper for ea...
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But I don't know why get relatively output? And have you met similar problem?
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Regarding when to use SVA - thanks, helpful to have an example for how it is deployed. I think I'...
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Hi h.mon, it worked wonderfully, now I have over 80% unique maps! thanks again!
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Thank you so much for your detailed answer! I'll address different parts of your post in unique c...
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Hello Shello, now we are back to the questions I asked at the very [beginning][1]. And: What kin...
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It's most likely 15M per end, which is on the low end. As reads can be of varying lengths, I pref...
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The starting point to any RNA-seq experiment should be a well-designed study that negates the nee...
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