Here we present a strategy for DNA sequencing, ECC sequencing, that can greatly improve sequencing accuracy and read length using a dual-base flowgram combined with fluorogenic SBS chemistry.

A new tool to predict the chances of successfully inserting a gene-edited sequence of DNA into the genome of a cell, using a technique known as prime editing, has been developed by researchers at ...

Caption Researchers at EMBL’s European Bioinformatics Institute (EMBL-EBI) have developed a new machine learning method called SAVANA that significantly reduces sequencing errors for cancer genomes.

A giant leap for genome sequencing as computerized method gives scientists a clearer view of DNA puzzles Johns Hopkins computer scientist Michael Schatz leads work on new algorithms for more complete ...

Nanopore DNA sequencing is a cutting-edge technology that enables the direct, real-time analysis of long DNA or RNA fragments. Unlike conventional sequencing methods that require the amplification and ...

This ability to cut any chosen DNA sequence can be used for gene editing; in tandem with other enzymes and/or DNA sequences, it can be used to insert or delete additional short sequences ...

Next-generation sequencing (NGS) has made analyzing DNA faster and cheaper, with effects felt in the lab, clinic, and beyond. A set of newly-launched technologies are offering a twist on the ...

For critically ill individuals, quick sequencing can be crucial for determining if the cause of life-threatening conditions are genetic. Another goal is to make it possible for any person, not just ...

The sequence data generated by one of these projects consists of millions or billions of short DNA sequences (reads) that range from 50 to 150 nt in length.

A new ultra-rapid genome sequencing approach developed by Stanford Medicine scientists and their collaborators was used to diagnose rare genetic diseases in an average of eight hours — a feat ...