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by Arbag
05-15-2019, 07:38 AM
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by eab
05-14-2019, 12:11 PM
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3,344 views
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by HelenaSC
05-13-2019, 01:06 AM
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10,026 views
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by SCIL2019
05-07-2019, 11:32 AM
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10 responses
9,485 views
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by SUKALPA
05-01-2019, 04:14 AM
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1,260 views
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by rlangley24
04-26-2019, 07:07 AM
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by JTH-Genome
04-24-2019, 10:53 AM
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by Him26
04-23-2019, 06:38 PM
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No topics found.
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Childhood cancers, effectively fatal 60 years ago, are now curable for up to 85% of children with access to contemporary treatments and...05-08-2026, 01:42 AM
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I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
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Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
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With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.
Introduction
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