Genome-wide association and MaODR-based multi-locus interaction analyses reveal a susceptibility gene network for newly identified metabolic syndrome [0.03%]
全基因组关联和MaODR-Based多基因位点相互作用分析鉴定出一组新的代谢综合征易感基因网络
Yu-Da Lin,Kuei-Hau Luo,Li-Yeh Chuang et al.
Yu-Da Lin et al.
Background: Metabolic syndrome involves several lipid-related genes, including apolipoprotein A5 (APOA5), lipoprotein lipase (LPL), and cholesteryl ester transfer protein (CETP). Although individual SNP susceptibility has...
Publisher Correction: Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants [0.03%]
publisher correction: 在 44,287 名多祖先参与者中分析肺功能和慢性阻塞性肺疾病的全基因组序列
Wonji Kim,Xiaowei Hu,Kangjin Kim et al.
Wonji Kim et al.
Published Erratum
Genome biology. 2026 Jun 9;27(1):189. DOI:10.1186/s13059-026-04141-8 2026
DNA methylation-based immune cell profiling in mouse blood using MouseRS-CMD [0.03%]
基于DNA甲基化的免疫细胞谱分析：小鼠血液中CMD的MouseRS检测法
Samuel R Reynolds,Hannah G Stolrow,Min Kyung Lee et al.
Samuel R Reynolds et al.
We present MouseRS-CMD, a murine DNA methylation-based immune cell deconvolution tool. Neutrophils, monocytes, natural killer cells, B cells, CD4 + and CD8 + T cells were purified. DNA methylation was measured with the Illumina Mouse Methyl...
TestNet: a method for inferring microbial networks with false discovery rate control for clustered and unclustered samples [0.03%]
测试微生物网络推断方法及聚类和非聚类样本的假发现率控制
Chang Su,Yicong Mao,Mengyu He et al.
Chang Su et al.
Most existing methods for inferring microbial networks generate only point estimates of Pearson's correlations without assessing their significance, and none accounts for clustering. We introduce TestNet, a novel method that delivers well-c...
Benchmarking reveals the superiority of nucleic acid foundation models in predicting lncRNA coding potential [0.03%]
基准测试揭示了核酸基础模型在预测长链非编码RNA编码潜力方面的优势
Yu Yang,Liping Ren,Juan Feng et al.
Yu Yang et al.
Background: A subset of long noncoding RNAs (lncRNAs) contains short open reading frames and can encode functional micropeptides. However, identifying these coding lncRNAs (codlncRNAs) remains challenging due to weak codi...
Evidence for G6PD variant classification from multiplexed functional assays [0.03%]
基于多重功能测定的G6PD变异分类证据
Renee C Geck,Melinda K Wheelock,Rachel L Powell et al.
Renee C Geck et al.
Background: G6PD deficiency is one of the most common enzyme deficiencies worldwide, and increases the likelihood of adverse reactions to certain drugs and foods. As availability of routine sequencing and biobanking incre...
Dbp7 interacts with RNA exosome component Dis3 to mediate CENP-A loading to centromeres [0.03%]
Dbp7通过与RNA外切酶组分Dis3的相互作用介导CENP-A在着丝粒上的加载
Jinxin Gao,Fengying Gao,Qianhua Dong et al.
Jinxin Gao et al.
Background: Centromeres are crucial for proper chromosome segregation during cell division. Centromeres in most eukaryotes are epigenetically defined by the histone H3 variant, CENP-A. Centromeric regions are typically tr...
pAnno: a comprehensive, precise, and fast proteogenomic workflow for the discovery of novel coding regions [0.03%]
pAnno：一种全面、精确且快速的蛋白质组学工作流程，用于发现新的编码区
Kaifei Wang,Zhuohong Wei,Changrong Li et al.
Kaifei Wang et al.
Proteogenomics is a transformative approach for deciphering novel coding regions through integration of genomic, transcriptomic, and proteomic data. Here, we present pAnno, an end-to-end workflow designed to uncover hidden protein-coding el...
Publisher Correction: Single-cell epigenetic and transcriptomic states across the continuum of monoclonal B cell lymphocytosis to chronic lymphocytic leukemia [0.03%]
出版更正：从单克隆B细胞淋巴细胞增多症到慢性淋巴细胞性白血病的单细胞表观遗传和转录组状态连续性研究
Anja C Rathgeber,Stacey M Fernandes,Adi Nagler et al.
Anja C Rathgeber et al.
Published Erratum
Genome biology. 2026 Jun 2;27(1):181. DOI:10.1186/s13059-026-04135-6 2026
Hybrid untargeted short-read and targeted long-read RNA sequencing facilitates genotype-phenotype associations at single-cell resolution [0.03%]
基于短读和靶向长读RNA测序的杂交无靶标单细胞基因型与表型关联分析
Jiayi Wang,Maria Constanza Maldifassi,Anna Bratus-Neuenschwander et al.
Jiayi Wang et al.
Long-read single-cell RNA sequencing enables simultaneous and unbiased detection of transcriptomic variants and gene expression, but its application is limited by low read coverage, restricting genotype-phenotype analyses at single-cell res...