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Unravelling the complexity of cancer genomics and predisposition: nanopore sequencing and the potential for personalised care | Oxford Nanopore Technologies
- Gene fusions
- Cancer research
- Clinical research
- Human genomics
- Structural variation
- Methylation
- DNA
- Adaptive sampling
- Targeted
- Whole genome
October 17 2024
Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanisms
- Gene fusions
- Cancer research
- Clinical research
- Human genomics
- Single cell
- Transcriptome
- cDNA
- RNA
- Variant calling
- Targeted
February 13 2024