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1474 results

Full text 2025

Whole genome sequence data of <i>Comamonas sediminis</i> FS4_11, a fumonisin B1-transforming bacterium, using hybrid nanopore-illumina sequencing

Wang Y, Zhao M, Wang Z, et al.

The genome of Comamonas sediminis FS4_11, a bacterial strain with mycotoxin fumonisin B1 (FB1) transformation capability, was sequenced using Oxford Nanopore Technologies (ONT) and Illumina platforms. The final assembly generated a circular chromosome of 5,148,490 …

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Nanopore Sequencing
Full text 2025

An allele-resolved nanopore-guided tour of the human placental methylome

Kindlova M, Byrne H, Kubler JM, et al.

The placenta is a temporary organ present during pregnancy that is responsible for coordinating all aspects of pregnancy between the mother and fetus. It has a distinct epigenetic, transcriptomic, and mutational landscape with low levels …

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Epigenetics Nanopore Sequencing Transcriptomics
Full text 2026

EASY-C: Extraction and Analysis of Small Yeast Chromosomes-A rapid and universal platform for recovering artificial mini-chromosomes from synthetic Sc2.0 yeast and large plasmids from <i>Saccharomyces cerevisiae</i> and nonconventional yeast species

Swidah R, Monti M, Delneri D.

The protocol for Extraction and Analysis of Small Yeast-Chromosomes (EASY-C) is a transformative, rapid, cost-effective, and user-friendly method designed for the efficient isolation of artificial synthetic mini-chromosomes (~42-52 kb) and large plasmids (~12 kb) from …

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Nanopore Sequencing
Full text 2025

Complete genome sequences of <i>Micrococcus luteus</i> isolated from the radioactive element-containing water in Fukushima Daiichi nuclear power station unit 2

Dotsuta Y, Taniguchi I, Gotoh Y, et al.

Four bacterial strains with yellow-colored colonies, which were isolated from the radioactive element-containing water in Fukushima Daiichi nuclear power station unit 2, were identified as <i>Micrococcus luteus</i>. Here, we present the complete genome sequences of …

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Nanopore Sequencing
Full text 2025

A new compression strategy to reduce the size of nanopore sequencing data

Jayasooriya K, Jenner SP, Marasinghe P, et al.

Nanopore sequencing is an increasingly central tool for genomics. Despite rapid advances in the field, large data volumes and computational bottlenecks continue to pose major challenges. Here, we introduce ex-zd, a new data compression strategy …

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Nanopore Sequencing
Full text 2026

De novo genome assembly of Ansell's mole-rat (Fukomys anselli)

Bekavac M, Coimbra R, Busa VF, et al.

Ansell's mole-rat (Fukomys anselli) is an African rodent known for its subterranean lifestyle and unique phenotypic traits, including extreme longevity, magnetoreception, and a cooperative breeding social structure. Efforts to dissect the genetic architecture of these …

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Nanopore Sequencing
Full text 2026

Decentralized nanopore genomics reveals diverse &lt;i&gt;Klebsiella pneumoniae&lt;/i&gt; and no evidence of patient-patient transmission in a New Zealand hospital

White RT, Bakker S, Burton M, et al.

<i>Klebsiella pneumoniae</i> is a leading cause of healthcare-associated infections worldwide, yet its population structure and transmission dynamics remain largely uncharacterized in New Zealand hospitals. We conducted a 15-month prospective genomic surveillance pilot at Wellington Regional …

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Nanopore Sequencing
Full text 2026

Genomic profiling of a DICER1-wildtype thyroblastoma reveals AGK-BRAF fusion, EIF1AX duplication, and TERT promoter mutations: integrated genomic and pathway analysis

Gualandi A, Picozzi F, Di Mauro A, et al.

<h4>Introduction</h4>Thyroblastoma is a rare and highly aggressive embryonal thyroid malignancy typically associated with DICER1 alterations. However, DICER1-wildtype cases remain poorly characterized at the molecular level.<h4>Methods</h4>We report a case of aggressive thyroblastoma in a 62-year-old male, …

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Nanopore Sequencing
Full text 2026

Detecting foldback artifacts in long-reads

Heinz JM, Meyerson M, Li H.

Long-read sequencing data is useful for detecting large and complex structural variations; however, technical artifacts can lead to false structural variant calls. In our analyses, we became aware of a foldback artifact in long-read data. …

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Nanopore Sequencing
Full text 2026

From High-Density Genomic Mapping to Precision Molecular Breeding: A Comprehensive Review of &lt;i&gt;Capsicum&lt;/i&gt; Genomic Resources

Wang L, Kan J, Zhong W, et al.

The genus <i>Capsicum</i> comprises several species that are vital vegetable and spice crops cultivated worldwide, possessing significant economic, nutritional, and ornamental value due to their diverse fruit morphologies, colors, spiciness levels, and stress resistance. Historically, …

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Genome Assembly Nanopore Sequencing Structural Variants
Full text 2026

A universal indel filtering workflow for both long-read and short-read NGS data

Bhuyan MSI, Rahman MS.

Accurate detection of insertions and deletions (indels) is critical for applications in disease genomics, population genetics, and personalized healthcare. Despite advancements in sequencing technologies, indel detection remains challenging, particularly in difficult-to-map genomic regions. In this …

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Nanopore Sequencing Structural Variants