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Protocol for mapping the three-dimensional organization of dinoflagellate genomes.


ABSTRACT: Dinoflagellate genomes often are very large and difficult to assemble, which has until recently precluded their analysis with modern functional genomic tools. Here, we present a protocol for mapping three-dimensional (3D) genome organization in dinoflagellates and using it for scaffolding their genome assemblies. We describe steps for crosslinking, nuclear lysis, denaturation, restriction digest, ligation, and DNA shearing and purification. We then detail procedures sequencing library generation and computational analysis, including initial Hi-C read mapping and 3D-DNA scaffolding/assembly correction. For complete details on the use and execution of this protocol, please refer to Marinov et al.1.

SUBMITTER: Marinov GK 

PROVIDER: S-EPMC10950746 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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Protocol for mapping the three-dimensional organization of dinoflagellate genomes.

Marinov Georgi K GK   Kundaje Anshul A   Greenleaf William J WJ   Grossman Arthur R AR  

STAR protocols 20240312 2


Dinoflagellate genomes often are very large and difficult to assemble, which has until recently precluded their analysis with modern functional genomic tools. Here, we present a protocol for mapping three-dimensional (3D) genome organization in dinoflagellates and using it for scaffolding their genome assemblies. We describe steps for crosslinking, nuclear lysis, denaturation, restriction digest, ligation, and DNA shearing and purification. We then detail procedures sequencing library generation  ...[more]

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