Hey everyone, is it possible to use sonication to break only base pairs but not phosphodiester bonds?
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I doubt it. The energy required to melt DNA or denature RNA is generally enough for phosphodiester bonds to start breaking (as evidenced by the fact that DNA and RNA don't store well at any temperature close to melting temperature). Sonication is commonly used for shearing DNA (at the phosphodiester bonds) for next-gen sequencing, which wouldn't work if the bases routinely broke from the phosphate/ribose backbone. I don't have a lot of experience with sonication, though, so I could be wrong.
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Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
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