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The paper identifies functional CREs in iPSCs and neurons and links them to neuropsychiatric disease risk variants.

This study shows that deleting subtelomeric X- and Y-elements in yeast does not affect telomere length or silencing, but impacts telomere maintenance when telomerase is inactivated.

This paper shows Kar4p is required for meiotic gene expression, with defects in early and late gene expression that can be partially rescued by overexpressing IME1 and RIM4.

The paper uses ancient DNA and genomic data to trace the genetic contributions of ancient farmer and steppe pastoralist lineages to the paternal genetic diversity of modern Chinese populations.

The paper shows that absence of Red1 and Hop1 recruitment prevents meiotic recombination on a chromosome arm containing the sex locus in Lachancea kluyveri, affecting genome evolution and fitness.

The paper shows ribose lowers RpoS levels via RbsD mRNA, which interacts with sRNAs DsrA and ArcZ, and requires Hfq.

The paper introduces LD graphical models (LDGMs) for efficient linkage disequilibrium representation in diverse ancestry studies, showing significant runtime improvements and better polygenic prediction.

The paper identifies genetic drivers of plasma lipoproteins in mice and links them to human lipid traits using QTL analysis and GWAS integration.

The paper identifies and characterizes two genes, Bcvic1 and Bcvic2, in Botrytis cinerea that are involved in vegetative incompatibility, a fungal allorecognition system.

The paper analyzes paleogenomic data from 5th-6th century Pannonia to reveal genetic diversity and migration patterns in post-Roman communities.

The paper identifies molecular signatures associated with russet skin formation in Niagara grapevine by analyzing transcriptomic and histological differences between somatic variants.

The paper identifies overexpression and nonsynonymous mutations in UGT genes associated with pyrethroid resistance in Anopheles funestus using GWAS-PoolSeq and transcriptomic analysis.

The paper identifies age-related increases in DNA methylation variability on the inactive X chromosome in females and males, with aVMCs accumulating in XCI regions and showing replication in purified cell types.

This study identifies six new quantitative trait loci influencing anterior chamber depth in mice using genetic crosses and QTL analysis.

The paper shows that Rtf2 in S. pombe is essential for proper splicing of Rtf1, which is necessary for RTS1 barrier activity.

This paper develops DeepGCF, a deep learning method to predict functional conservation between human and pig using epigenome and transcriptome data, showing improved performance and insights into regulatory and heritability patterns.

This paper introduces a deep learning tool for phenotyping 3D micro-CT data to support genetic analysis of morphological traits in fish.

This study compares seven genomic cross selection criteria to improve genetic gain and diversity in inbred plant breeding by evaluating their impact on progeny performance and genetic variance.

This study uses Genomic Structural Equation Modeling to identify a common genetic factor underlying externalizing phenotypes and substance use disorders, finding that a single dimension of genetic risk best explains their relationships.

The paper evaluates population structure inferred by PCA or admixture models by assessing model fit and identifying poorly represented individuals.