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Full text 2026

Light-based footprinting of a eukaryotic genome

Ögren L, Muylaert I, Elliott K, et al.

Identification of protein-bound DNA sites is key to understanding genome function and regulation, but studying protein-DNA interactions in living, unperturbed cells remains challenging. UV footprinting has been used to study such interactions in vivo by …

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Bioinformatics
Full text 2026

Integrative insights into abiotic stress tolerance in finger millet (<i>Eleusine coracana</i> (L.) Gaertn.): linking physiological, biochemical, and molecular perspectives for developing climate-smart cereals

Rakkammal K, Muthuramalingam P, Pandian S, et al.

Finger millet (<i>Eleusine coracana</i> (L.) Gaertn.) is a resilient yet underutilized cereal with exceptional potential to withstand adverse environmental conditions. Despite its adaptability, the genetic and physiological bases of its stress tolerance remain insufficiently characterized …

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Transcriptomics
Full text 2026

A genome assembly of the California poppy, Eschscholzia californica

Nguyen PT, Escalona M, Ryan E, et al.

The California poppy (Eschscholzia californica), a native wildflower of western North America and the state wildflower of California, is characterized by extensive ecological variation and adaptation to diverse climatic conditions. Its broad geographic range and …

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Genome Assembly
Full text 2026

Federated, governed, and interoperable? The emerging architecture of public human genomic data infrastructures: a European perspective

Tangaro MA, Chiara M, Pesole G, et al.

Public infrastructures for human genomic data are increasingly incorporating federated approaches alongside centralized and cloud-native models, yet operational federation remains constrained by unsolved challenges at the legal, semantic, and technical layers. We describe the current …

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Bioinformatics
Full text 2026

HMGCR genetic variation and risk of new-onset type 2 diabetes in statin users

Albawa'neh AS, Alqasrawi MN, Al-Mahayri ZN, et al.

BACKGROUND: Statins are widely prescribed lipid-lowering agents, but their use is associated with an increased risk of new-onset type 2 diabetes mellitus (NO-T2DM) ranging from 9% to 13%. While genetic variants in 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), …

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Epigenetics
Full text 2026

ClinGen API platform for classification of human genetic variants

Shah N, Farris T, Zuniga AA, et al.

In this commentary, we describe how the Clinical Genome Resource's (ClinGen's) application programming interface-based microservices accelerate growth and dissemination of knowledge about human genetic variation. By exposing findable, accessible, interoperable, reusable, and AI-ready variant data, …

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Bioinformatics