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Originally posted by lailaizhang View PostThanks. Looks like I should use the HS kit since my DNA is only about 5 ng/ul
I once ran out of the BR dsDNA assay which I had been using to measure the concentration of my RNAseq libraries for cluster concentration calculations and instead used a HS assay in a pinch, did the calculations the same and clustered at "the same" concentration and all my libraries over clustered. I then did a side by side of the libraries with the BR and HS and there was on average a 29% difference between the values given, with the BR being higher. All the libraries were falling in the 40ng/ul range on the HS so they were well with in the BR kit range
I had good consistent clustering results with the BR assay when using it, and only had a problem with it when i switched to HS without making adjustments for the different values given. (<-- unknown to me at the time, or an oversight) I will stick with HS from now on for anything under 100ng/ul, I do feel like it is more accurate with in that range vs the BRLast edited by subxero; 10-01-2015, 04:23 AM.
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