Haplotype-specific identification of genetic and epigenetic variation using nanopore sequencing
Join us for this Knowledge Exchange to learn how to accurately identify genetic and epigenetic variation in a single dataset
It takes two — haplotype-specific identification of genetic and epigenetic variation using nanopore sequencing
Using nanopore sequencing, researchers can achieve real-time, high-performance, accessible, and scalable analysis of DNA and RNA, with the added benefits of high-accuracy variant discovery, built-in methylation detection, and so much more.
To learn more, listen to Philipp Rescheneder discuss assigning variants to the correct haplotype through phasing, and how nanopore sequencing can improve the understanding of tumour development.
A guide to investigating methylation in the human genome
This guide provides an introduction to the direct sequencing of DNA methylation in human genomes – from designing your protocol, all the way through to analysing your data.
Methylation detection with nanopore sequencing
Our recent Knowledge Exchanges introduce Remora, for genome-wide methylation detection, and Reduced-Representation Methylation Sequencing, for targeted methylation detection.
Fully characterise human genetic variation with real-time nanopore sequencing technology
With nanopore technology, there is no limit to read length (current record >4 Mb), enabling complete resolution of challenging regions and uncovering previously hidden variation. Plus, you can identify base modifications as standard, with amplification-free native DNA or RNA sequencing.
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