Advancing human genomics with nanopore sequencing
High-throughput sequencing technologies have revolutionized the field of human genetics, allowing researchers to further our understanding of biological processes and their impact. However, the use of traditional short-read sequencing technologies presents many limitations, including the inability to analyze repeat regions, structural variants, phasing, full-length transcript isoforms, and methylation.
This White Paper describes how researchers are now utilizing nanopore sequencing to overcome these challenges, to deliver a more comprehensive understanding of the human genome and genetic diseases.
In this White Paper, learn more about:
- Direct RNA sequencing
- Advancing dementia research through comprehensive analysis of large cohorts
- New insights into human transcriptome variation
And much more!
This content was provided by Oxford Nanopore Technologies
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