Blog
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Short, long, or ultra-long: which read length is right for you?
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Pushing the boundaries of rare disease research
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Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanisms
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Characterising alternative splicing in the human cortex with ultra-deep nanopore sequencing
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London Calling 2024 opens with a day of masterclasses delivering everything you need to know for sample-to-answer nanopore sequencing
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cDNA and RNA sequencing: revealing the transcriptome
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Adaptive sampling: redefining targeted sequencing
