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STAR Protoc ; 1(3): 100123, 2020 12 18.
Article in English | MEDLINE | ID: mdl-33377017

ABSTRACT

Dual RNA-sequencing is a powerful technique to assess both bacterial and host transcriptomes in an unbiased way. We developed a protocol to perform Dual RNA-seq on in vivo-derived macrophage populations infected with Mycobacterium tuberculosis. Here, we provide a practical step-by-step guide to execute the protocol on Mtb-infected cells from a murine infection model. Our protocol can also be easily applied to perform Dual RNA-seq on in vitro-derived cells as well as different Mtb-infected host cell types. For complete details on the use and execution of this protocol, please refer to Pisu et al. (2020).


Subject(s)
Mycobacterium tuberculosis/genetics , RNA-Seq/methods , Sequence Analysis, RNA/methods , Animals , Base Sequence/genetics , Disease Models, Animal , Gene Expression Profiling/methods , Host-Pathogen Interactions/genetics , Macrophages/metabolism , Mice , Mycobacterium tuberculosis/isolation & purification , Mycobacterium tuberculosis/pathogenicity , RNA/metabolism , Transcriptome/genetics , Tuberculosis/diagnosis , Tuberculosis/genetics , Tuberculosis/metabolism
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