When we sequence BAC library using NGS, how many clones should we mix? When we use 454 to do it, can we mix 6 or 12 clones to sequence a full run? And if we use illumine how many can we mix? Thank you!
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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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