I am trying to run conifer and not sure about the SVD normalization like how its is done. How the sample amount effects the analysis quality. what does removal of svd components mean. while calling CNV how on what basis do we set the threshold value? How can we measure the sensitivity and the specificity of the result.
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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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