Chromatin Immunoprecipitation for Identification of Protein–DNA Interactions in Human Cells

Author(s):  
Bjørk Ditlev Larsen ◽  
Martin Rønn Madsen ◽  
Ronni Nielsen ◽  
Susanne Mandrup
2004 ◽  
pp. 129-146 ◽  
Author(s):  
Hogune Im ◽  
Jeffrey A. Grass ◽  
Kirby D. Johnson ◽  
Meghan E. Boyer ◽  
Jing Wu ◽  
...  

2020 ◽  
Vol 1 (1) ◽  
pp. 100020
Author(s):  
Wim J. de Jonge ◽  
Mariël Brok ◽  
Patrick Kemmeren ◽  
Frank C.P. Holstege

2008 ◽  
Vol 5 (4) ◽  
pp. 307-309 ◽  
Author(s):  
Nathaniel D Maynard ◽  
Jing Chen ◽  
Rhona K Stuart ◽  
Jian-Bing Fan ◽  
Bing Ren

2020 ◽  
Author(s):  
L. Arrigoni ◽  
F. Ferrari ◽  
J. Weller ◽  
C. Bella ◽  
U. Bönisch ◽  
...  

ABSTRACTChromatin immunoprecipitation followed by sequencing (ChIP-seq) is a method used to profile protein-DNA interactions genome-wide. RELACS (Restriction Enzyme-based Labeling of Chromatin in Situ) is a recently developed ChIP-seq protocol that deploys a chromatin barcoding strategy to enable standardized and high-throughput generation of ChIP-seq data. The manual implementation of RELACS is constrained by human processivity in both data generation and data analysis. To overcome these limitations, we have developed AutoRELACS, an automated implementation of the RELACS protocol using the liquid handler Biomek i7 workstation. We match the unprecedented processivity in data generation allowed by AutoRELACS with the automated computation pipelines offered by snakePipes. In doing so, we build a continuous workflow that streamlines epigenetic profiling, from sample collection to biological interpretation. Here, we show that AutoRELACS successfully automates chromatin barcode integration, and is able to generate high-quality ChIP-seq data comparable with the standards of the manual protocol, also for limited amounts of biological samples.


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