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1474 results

Full text 2026

A bench-to-data analysis workflow for respiratory syncytial virus whole-genome sequencing with short and long-read approaches

Gómez-Del Rosario A, Muñoz-Barrera A, Alcoba-Florez J, et al.

Genomic surveillance of respiratory syncytial virus (RSV) enables detecting and monitoring of circulating lineages and the emergence of amino acid substitutions affecting transmission, severity, and treatment. We present a comprehensive workflow for RSV whole-genome sequencing, …

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Nanopore Sequencing
Full text 2026

High-quality metagenome assembly from nanopore reads with nanoMDBG

Benoit G, James R, Raguideau S, et al.

Third-generation long-read sequencing technologies, significantly improve metagenome assemblies. Highly accurate PacBio HiFi reads can yield hundreds of near-complete metagenome-assembled genomes (MAGs) from a single sample. Recently, the accuracy of the more cost-effective Oxford Nanopore Technologies …

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Nanopore Sequencing
Full text 2025

Targeted next-generation sequencing for drug-resistant tuberculosis diagnosis: implementation considerations for bacterial load, regimen selection and diagnostic algorithm placement

Georghiou SB, Tukvadze N, Rodrigues C, et al.

<h4>Introduction</h4>Early and accurate diagnosis of drug-resistant tuberculosis (DR-TB) is essential for improving treatment outcomes. Phenotypic drug susceptibility testing (pDST) is comprehensive but slow, while rapid molecular assays provide resistance information for a limited number of …

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Nanopore Sequencing
Full text 2026

Evaluating Sequencing Strategies for Endometrial Microbiome Profiling in Endometrial Cancer: A Comparative Study of Short- and Long-Read 16S rRNA Approaches

Bebelman S, Artuyants A, Nijmeijer B, et al.

<h4>Background</h4>Endometrial cancer (EC) is the most common gynaecological malignancy globally, with rising incidence and notable disparities in outcomes. In New Zealand, EC rates have increased significantly, particularly among Māori and Pacific women, who face higher …

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Nanopore Sequencing
Full text 2026

Nallo: a Nextflow pipeline for comprehensive human long-read genome analysis

Lenner F, Jemt A, Peña Pérez L, et al.

<h4>Motivation</h4>Long-read sequencing (LRS) is increasingly used for human medical research and clinical diagnostics due to its capacity to generate complete genome information. However, there is a lack of robust and easy-to-use pipelines for comprehensive LRS …

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Nanopore Sequencing
Full text 2026

A course-based undergraduate research experience (CURE) designed for modern genetics and biodiversity courses using a classroom benchtop sequencer

Ebbs ET, Barredo A, Whitehurst A, et al.

Modern genetics increasingly relies on genomic data sets to address medical, ecological, and evolutionary questions. Investigating these questions requires a diverse set of core competencies in wet-lab techniques, data analysis, and bioinformatics. We describe the …

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Nanopore Sequencing
Full text 2026

Chromosome-level genome assembly of the sponge Halisarca dujardinii

Zubarev V, Cherkasov A, Sidorov L, et al.

Halisarca dujardinii is a marine sponge known for its ability to completely regenerate via cell reaggregation. Here we present the first chromosome-level genome assembly of H. dujardinii, generated using Oxford Nanopore long reads, Illumina short …

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Nanopore Sequencing
Full text 2026

Rapid Sequence Identification of Foot-and-Mouth Disease Virus Utilizing FMDV-ONTAPS: The Oxford Nanopore Technologies Amplicon P1 Sequencing Protocol

Yeo S, Hole K, Chestley T, et al.

Diagnostic testing of foot-and-mouth disease virus (FMDV) currently utilizes reverse transcription quantitative PCR (RT-qPCR) to detect the presence of viral RNA and double antibody sandwich ELISAs (DAS-ELISAs) to determine viral serotype. Serotype identification is critical …

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Nanopore Sequencing