We are in the process of validating the PGM and any data you would be willing to share in which the mutation was detected by the PGM and confirmed by sanger? Please contact me if you are able yo share the FASTQ and BED.I thank you for your assistance in the validation process.
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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...
