Has anyone had any experience troubleshooting extremely low intensities after running the first base chemistry on the GAII. The low intensities continue throughout the run and its not necessarily every lane displaying the lowered intensities depsite the same sample, with the same dilution, in the lanes. I understand focusing can be an issue with this, it's not in this case. I'm reasonably confident the cluster generation is not at issue. I've heard people suggest that if you see low intensities that you should strip off the sequncing primer and rehyb. Anyone who's tried that? what kind of results are you getting by doing that? Thanks for any assitance you guys can provide.
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by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
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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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