What is low-coverage genome sequencing? Genotypes detected using high-depth resequencing methods are undoubtedly the most comprehensive, but are currently too...
Illumina’s Next-Generation Sequencing (NGS) workflow is a sophisticated and highly efficient process that enables researchers to unravel the mysteries of...
Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq) is a powerful technique in epigenomics, allowing researchers to study chromatin accessibility. ATAC-seq...
Introduction In the realms of functional genomics and epigenetics, the elucidation of transcription factor binding sites (TFBS) has perennially stood...