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 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 ...

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 ...

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.

Instead, adaptive sequencing eliminates hours of watching irrelevant content by quickly recognizing unwanted movies and skipping to the next entry. The open-source software's algorithm was written by ...

The new development combines the advantages of the most advanced tools for working with genomic data. The new method will enable scientists to analyze DNA sequences faster and more accurately and ...

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 ...

Scientists propose an algorithm to study DNA faster and more accurately Date: January 19, 2016 Source: Moscow Institute of Physics and Technology Summary: The new development combines the ...

Genome Research publishes Part 2 of the Special Issue on Long-read DNA and RNA Sequencing Applications in Biology and Medicine, a diverse collection of research, methods, and review articles ...

Roche has put forward a new approach to genetic analysis, which it describes as sequencing-by-expansion—a proprietary method that pulls apart the DNA molecule and amplifies the signal of each ...

Researchers have developed a new machine learning algorithm, SAVANA, which can accurately identify cancer-specific structural variations and copy number aberrations in long-read DNA sequencing data, ...