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I downloaded all the data, and used perl version to test with the default parameter(only changed the path). Pf was set to 0 according to the paper. My sgr files were the same as that of the website. But I got a different result. The final regions are different from 24,739 in the paper. Does anyone test this? And whether there are other parameters i haven't considered? Thank you so much!
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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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10-14-2026, 09:55 AM -
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by SEQadmin2
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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Started by SEQadmin2, 10-22-2026, 11:13 AM
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10-22-2026, 11:13 AM
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Started by SEQadmin2, 10-22-2026, 10:48 AM
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10-22-2026, 10:48 AM
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Started by SEQadmin2, 10-15-2026, 10:52 AM
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Started by SEQadmin2, 10-14-2026, 05:39 AM
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10-14-2026, 05:39 AM
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