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2014): Biochemical methods, such as ChIP or DNase hypersensitivity assays, capture extended regions of several hundred bases, whereas the underlying transcription factor binding elements are typically only 6 15 bp in length.
Biochemical methods, such as ChIP or DNase hypersensitivity assays, capture extended regions of several hundred bases, whereas the underlying transcription factor binding elements are typically only 6 15 bp in length.
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These elements are typically up to 500 bp long and contains binding sites for sequence-specific several distinct transcription factors [ 8].
The masses of chemical elements are, typically, thousands of MeV (million electron volts, in energy units), while the kinetic and binding energies are a few tens of electron volts.
These elements are typically called national extensions.
Therefore, other elements are typically contrasted with this option.
Now, off-diagonal elements are typically only one order of magnitude smaller than diagonal elements.
These rearrangements are believed to be created by IS-elements and the elements are typically flanked by pseudogenes [ 8- 10].
This is not surprising as such extra-chromosomal elements are typically lost in cell culture.
In stenotrophomonads, REP elements were typically found in tens or a few hundred copies per genome.
A stochastic processing element is typically implemented by a logic gate.
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