The most comprehensive insight into cancer genomes
The unique attributes of nanopore sequencing can fully address the limitations of traditional sequencing technologies, so researchers can achieve the most comprehensive insight into cancer genomes. This includes the ability to resolve variants and epigenetic modifications, target large panels or single genes without PCR, and detect full-length transcripts with single-cell resolution.
For more information, check out:
- White paper: Accelerating cancer research through comprehensive genomic analysis
- Case study: Rapid, low-cost detection of genomic aberrations
- Talk: Identification of novel genomic structures and regulation patterns at HPV integration events in cervical cancer
- Case study: Promising potential for non-invasive cancer monitoring
This video was provided by Oxford Nanopore.
Submit Your Research to the F1000Research Genomics & Genetics Gateway
Advance the fields of genomics and genetics by publishing your research with the F1000Research Genomics & Genetics Gateway. With trusted publishing, open access, and transparent peer review, your work will uphold the highest standards of rigor and integrity while driving innovation in PCR, sequencing, and genetic analysis.
Join a platform that values transparency, openness, and author control. Submit your research today at F1000Research Genomics & Genetics Gateway.
