Results 221 to 230 of about 65,196 (347)
Rapid reconstruction of multidrug‐resistant bacterial genomes using CycloneSEQ nanopore sequencing
Multidrug‐resistant (MDR) bacteria commonly harbor highly complex genomes enriched with mobile elements and resistance islands, which are challenging to resolve using short‐read sequencing. Here, we evaluated CycloneSEQ, a newly developed Chinese nanopore sequencing platform, for MDR genome reconstruction.
Kai Peng +9 more
wiley +1 more source
A new bioinformatics pipeline called ECCFP has been developed to improve the detection of extrachromosomal circular DNA (eccDNA) from long‐read sequencing data. ECCFP uses all consecutive full passes from individual reads for candidate eccDNA identification and consolidates candidate eccDNAs to generate accurate unique eccDNA.
Wang Li +14 more
wiley +1 more source
A comprehensive benchmarking of adaptive sampling tools for nanopore sequencing. [PDF]
Yang L +9 more
europepmc +1 more source
Fast bootstrap and reliable readout using hidden references for DNA data storage
This study provides a bootstrap readout framework for DNA data storage based on multiple‐fold hidden references. We employ a multi‐stage alignment and error correction strategy, transforming the de novo readout into a resequencing‐like workflow. Correlation to the hidden watermark reference identifies low‐error‐rate reads, and bit‐wise consensus ...
Weigang Chen +6 more
wiley +1 more source
Evaluation of a Probe-Based Enrichment Protocol for Nanopore Sequencing of Zoonotic Viruses. [PDF]
Hawes K +9 more
europepmc +1 more source
Majorbio Cloud 2026 provides comprehensive analysis workflows for microbiome
The integrated microbiome data analysis platform on Majorbio Cloud (https://cloud.majorbio.com/) encompasses 26 analytical workflows, with a core architecture of two modules: single‐omics workflows and cross‐omics integration and correlation workflows.
Jianhua Zhao +14 more
wiley +1 more source
Exploiting nanopore sequencing advances for tRNA sequencing of human cancer models. [PDF]
Kochavi A +6 more
europepmc +1 more source
This study reports a de novo MAGEL2 pathogenic variant in a patient with Schaaf–Yang syndrome, confirmed through methylation‐sensitive analysis. Combining genomic sequencing with methylation assays helps accurately determine the parental origin of MAGEL2 mutations.
Youn‐Ji Hong +7 more
wiley +1 more source
Employing nanopore sequencing on FFPE-derived DNA for CNS tumor diagnostics. [PDF]
Kerbs P +22 more
europepmc +1 more source

