Blog
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Revealing hidden genetic variants in rare disease with nanopore sequencing
- SNVs
- Clinical research
- Variant calling
- Human genomics
- Structural variation
- Epigenetics
October 26 2023
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Pushing the boundaries of rare disease research
- SNVs
- Clinical research
- Human genomics
- Whole genome
- Targeted
- PromethION
June 6 2023
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At London Calling 2024, the Nanopore Community showcases how ‘nanopore sequencing can drive new discoveries in biology’
- SNVs
- Bacteria
- Cancer research
- Clinical research
- Conservation
- DNA
May 23 2024