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The paper identifies novel structural variants and archaic introgressions in Tibetan genomes linked to high-altitude adaptation.

The paper develops a cross-ancestry information transfer framework to improve protein abundance prediction and protein-trait association identification in underrepresented populations.

This study presents a high-quality genome assembly of Anolis distichus, revealing insights into neo-sex chromosome evolution and differential evolutionary pressures.

This study identifies genetic variants associated with longevity in a Calabrian cohort, finding one genome-wide significant variant and highlighting pathways related to aging.

This paper develops a federated framework for GWAS using mixed-effects models to enable privacy-preserving analysis across distributed datasets while maintaining statistical accuracy.

The paper presents chromosome-level genome assemblies of four Diamesa species, revealing gene family contractions and expansions linked to cold tolerance and high-altitude adaptations.

Pf-PeptideFilter is a web-based tool that filters peptide vaccine candidates for Plasmodium falciparum using genomic and transcriptomic data to prioritize immunogenic targets.

The paper presents a chromosome-level genome assembly for the rare lava gull using Oxford Nanopore sequencing, providing a resource for phylogeography and population genetics studies.

CRYPTID-exon identifies cryptic exons in human RNA-seq data, showing their impact on mRNA stability and gene expression through ASO targeting.

The paper analyzes DEF and anti-DEF gene dynamics across Enterobacteriaceae genomes, finding differences in turnover rates between chromosomal and mobile genetic elements.

This study shows H19 upregulation in HLHS impairs mitophagy and increases ischemic vulnerability in immature hearts and cardiomyocytes.

Enigma is an efficient regulatory genomics model that achieves competitive performance with state-of-the-art models while significantly reducing computational cost.

The paper develops CAGEs to enable high-throughput multi-step assays on live cells, measuring gene expression persistence in expanding clones.

The paper investigates DNA methylation patterns in human bronchial epithelial cells and identifies chromatin determinants that influence their establishment.

This study presents a chromosome-level genome of Ditylenchus destructor and identifies stage-specific effectors and transcription factors critical for parasitism.

This study uses forensic genetic techniques to identify Columbus descendants from archaeological remains through familial relationship analysis.

This study identifies over 2,000 GC-responsive non-coding transcripts across nine human cell types, revealing cell-type-specific regulation of lncRNAs and miRNAs.

This paper introduces a semi-permeable capsule technology for high-throughput single-cell -omics, demonstrating its utility in scRNA-Seq of hematopoietic disorders and uncovering transcriptome changes in AML.

This study sequences the complete mitochondrial genome of Hanabira yukibana, finding it to be 18,690 bp with 17 genes and gene order pattern A, supporting its placement with the genus Clavularia.

This study identifies IS1216 as a key driver in the evolution of pRUM-like multidrug resistance plasmids in Enterococcus faecium through comparative genomic analysis of 152 plasmid sequences.