Abstract: Motivated by duplex read sequencing developed by Oxford Nanopore Technologies, this paper proposes a concatenated coding scheme for nanopore sequencers where DNA sequences are decoded from ...

Our free RNA Reverse Complement tool helps researchers and students who work with RNA sequences. You can use it to analyze transcript data, design siRNAs, or study viral genomes. Just enter your FASTA ...

Abstract: This paper presents constructions of DNA codes that satisfy biological and combinatorial constraints for DNA-based data storage systems. We introduce an algorithm that generates DNA blocks ...

Neuronal injury in autoimmune encephalitis (AE) may involve antibodies or T cells, with or without complement activation. Cell-free DNA (cf-DNA), released during cell death, and the complement split ...

Our free DNA Reverse Complement tool is an indispensable utility for researchers, students, and technicians in molecular biology and genomics. Whether you’re designing PCR primers, verifying ...

DNA storage represents a revolutionary approach to data archival, offering unprecedented storage density and longevity. This project implements the DNA Fountain algorithm, which combines fountain ...

DNA coding theory bridges the disciplines of mathematics, computer science and molecular biology by applying advanced algebraic and combinatorial techniques to the design of nucleotide sequences. This ...

For decades, the dream of fixing harmful mutations in mitochondrial DNA felt out of reach. Scientists have long known these mutations cause serious diseases that pass down only through mothers. They ...