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Human pluripotent stem cells can be differentiated into exocrine pancreas progenitor organoids, allowing studies of development and pancreatic cancer modeling.
A pipeline incorporating genetic fine mapping, epigenome editing, and genome editing enables functional analysis of disease-associated SNPs located in non-protein-coding regions of the genome.
A method for converting biopsy-size tissue samples into digital files containing the mass spectrometry–measurable proteome of the sample will allow analysis and re-analysis of limited tissue samples.