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1Program in Gene Function and Expression, Department of Biochemistry and Molecular Pharmacology,University of Massachusetts Medical School, 2Broad Institute of Harvard and Massachusetts Institute of Technology, 3Division of Health Sciences and Technology,Massachusetts Institute of Technology, 4Program for Evolutionary Dynamics, Department of Organismic and Evolutionary Biology, Department of Mathematics,Harvard University , 5Department of Applied Mathematics,Harvard University , 6Department of Physics,Massachusetts Institute of Technology, 7Department of Systems Biology,Harvard Medical School, 8Department of Biology,Massachusetts Institute of Technology
Capítulos
- 00:00Título
- 01:03Introduction
- 02:07Crosslinking, Digestion, Marking of DNA Ends, and Blunt-End Ligation
- 09:46Shearing and Size Selection
- 12:03Biotin Pull-Down and Paired End Sequencing
- 16:38Representative Hi-C Results
- 21:32Conclusion
La méthode Salut-C permet l'identification sans parti pris, l'ensemble du génome des interactions chromatine (1). Salut-C couples ligature de proximité et le séquençage massivement parallèle. Les données obtenues peuvent être utilisées pour étudier l'architecture génomique à plusieurs échelles: premiers résultats identifié des caractéristiques telles que les territoires chromosomiques, la ségrégation de la chromatine ouverte et fermée, et la structure de la chromatine à l'échelle mégabase.
