Are there any good comparison papers or studies between the Nextseq 2000 and the Novaseq X for WGS variant calling? Seems like there are several papers comparing the old Nextseq 550 platform but not much between these two platforms. Obviously they should be similar but the question is how similar for the exact same library.
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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...