A high-quality genome assembly of Silene latifolia was generated by researchers at CNRS/Université Claude Bernard Lyon 1 and ...

One in every 10 people worldwide is impacted by a rare genetic disease but about 50% of them remain undiagnosed despite rapid increases in genetic technology and testing.

Oxford Nanopore Technologies is looking forward ... s enough of an unmet need in what we do with the native DNA—whether it’s methylation, whether it’s point of care, time to result.

Scientists at deCODE genetics have unveiled a groundbreaking map of human DNA mixing during reproduction, offering insights into genetic diversity, health, and fertility. Credit: SciTechDaily.com ...

For mRNA vaccine development, Oxford Nanopore sequencing has been modified to sequence them directly without reverse transcription. Although the accuracy of direct sequencing of RNA is lower than that ...

Sichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences and Sichuan Provincial People ...

c) Programmable assembly of mobile DNA types carrying epi-bits. d) Parallel printing via DNMT1-guided catalysis to selectively write epi-bits. e) Nanopore sequencing of modified templates and ...

Dunn, recently carried out a study exploring how DNA methylation, an epigenetic modification that entails the addition of a methyl group to the DNA, contributes to the well-documented relationship ...

The results of this study were presented as a poster at The International Symposium on Health Informatics and Bioinformatics (HIBIT Bioinformatics) ...

While most known types of DNA damage are fixed by our cells' in-house DNA repair mechanisms, some forms of DNA damage evade repair and can persist for many years, new research shows.