NAR Genomics and Bioinformatics

Utilizing protein structure graph embeddings to predict the pathogenicity of missense variants.

Cluefish: mining the dark matter of transcriptional data series with over-representation analysis enhanced by aggregated biological prior knowledge.

A high-resolution meiotic crossover map from single-nucleus ATAC-seq reveals insights into the recombination landscape in mammals.

SeArcH schemes for Approximate stRing mAtching.

SLAYER: a computational framework for identifying synthetic lethal interactions through integrated analysis of cancer dependencies.

SLAYER：一种通过对癌症依赖性的综合分析来识别合成致死相互作用的计算框架

GEMCAT-a new algorithm for gene expression-based prediction of metabolic alterations.

GEMCAT——一种基于基因表达的代谢改变预测新算法

Identifying similar populations across independent single cell studies without data integration.

在不进行数据整合的情况下，识别独立单细胞研究中的相似细胞群

The divergent intron-containing actin in sponge morphogenetic processes.

海绵形态发生过程中含内含子的肌动蛋白的分化

Comparative analysis and classification of highly divergent mouse rDNA units based on their intergenic spacer (IGS) variability

基于基因间隔区 (IGS) 变异性对高度分化的小鼠 rDNA 单元进行比较分析和分类

A single-cell strategy for the identification of intronic variants related to mis-splicing in pancreatic cancer

一种用于识别胰腺癌错误剪接相关内含子变异的单细胞策略