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The sequencing depth is directly correlated with cost. If abundant binders in large genomes have to be mapped with high sensitivity, costs are high as an enormously high number of sequence tags will be required. This is in contrast to ChIP-chip in which the costs are not correlated with sensitivity. [12] [13]
A single sequencing run can scan for genome-wide associations with high resolution, due to the low background achieved by performing the reaction in situ with the CUT&RUN sequencing methodology. ChIP-Seq, by contrast, requires ten times the sequencing depth because of the intrinsically high background associated with the method. [6]
A single sequencing run can scan for genome-wide associations with high resolution, due to the low background achieved by performing the reaction in situ with the CUT&RUN-sequencing methodology. ChIP-Seq, by contrast, requires ten times the sequencing depth because of the intrinsically high background associated with the method. [7]
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The cost of acquiring a pH-mediated sequencer at time of launch was priced at around $50,000 USD, excluding sample preparation equipment and a server for data analysis. [8] [11] [15] The cost per run is also significantly lower than that of alternative automated sequencing methods, at roughly $1,000. [8] [12]
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