In a way, sequencing DNA is very simple: There's a molecule, you look at it, and you write down what you find. You'd think it would be easy—and, for any one letter in the sequence, it is. The problem ...

Viral DNA that is usually dismissed when sequencing the human genome could help to uncover useful information about complex ...

Readouts of the full DNA of children with cancer at diagnosis have been implemented as the standard of care in a European first. By determining a child's type of cancer as precisely as possible, the ...

Researchers are now exploring how to best extract and use saliva-derived DNA for long-read sequencing applications. Download ...

Companies unite in shared vision of enabling researchers to translate genomic insights to groundbreaking discoveries Partnership includes launch of new IDT xGen™ NGS products designed exclusively for ...

近期，香港城市大学李润生团队在bioRxiv预印本平台发表了一项系统比较研究，题为《When CycloneSEQ meets Oxford Nanopore Technologies: a performance comparison of contemporary nanopore DNA sequencing platforms》（Liu et al.）。该研究通过六种细菌样本的全基因组测序 ...

Miami University’s Center for Bioinformatics and Functional Genomics (CBFG) has become one of the first institutions in the region to acquire the PacBio VEGA Benchtop System — a cutting-edge DNA ...

As questions surrounding paternity fraud and DNA disputes gain prominence, experts maintain that despite the introduction of Next Generation Sequencing [NGS] Capillary Electrophoresis [CE] precision, ...

Saliva is an easily accessible source of high molecular weight DNA for Oxford Nanopore long-read sequencing applications.