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Methodological aspects of whole-genome bisulfite sequencing analysis
Exome sequence read depth methods for identifying copy number changes
Exploring the function of genetic variants in the non-coding genomic regions
Deciphering oncogenic drivers
Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits
An open-pollinated design for mapping imprinting genes in natural populations
Breast cancer classification
From miRNA regulation to miRNA–TF co-regulation
Current innovations and future challenges of network motif detection
Functional mapping of seasonal transition in perennial plants
Causes, consequences and solutions of phylogenetic incongruence