There are some good examples on how to make a single multiWig file for visualization with a UCSC track hub, but I have 48 multiWig's I would like to make (i.e. 48 tracks from 288 wig files). Does anyone have an example on how to set this up?
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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...
