本数据集是neXtProt癌症变体门户的核心数据，包含人类癌症相关蛋白质中遗传变体及人工突变体的功能影响注释信息。注释以三元组形式呈现，涵盖变体对象、功能影响关系及受测属性，可用于分析癌症相关蛋白质变体的生物学功能与表型关联。 SIB - Swiss Institute of Bioinformatics（瑞士生物信息学研究所）CALIPHO研究组
Genetic variants which affect complex traits (causal variants) are thought to be found in functional regions of the genome. Identifying causal variants would be useful for predicting complex trait phe
The European project AQUA-FAANG aims to improve understanding the genome function and usage of genotype-to-phenotype prediction in the six most important European farmed fish species. This study is pa
Associations between lifestyle and enrichment for functional divergence: the numbers of genomes in each category are given in the form Lifestyle/Comparison. Significance was assessed with Yates-correc
