RNA-Seq as a Tool to Study the Tumor Microenvironment

The transcriptome is composed of different types of RNA molecules including mRNAs, tRNAs, rRNAs, and other noncoding RNAs that are found inside a cell at a given time. Analyzing transcriptome patterns can shed light on the functional state of the cell as well as on the dynamics of cellular behavior...

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Veröffentlicht in:Methods in molecular biology (Clifton, N.J.) Jg. 1458; S. 311
Hauptverfasser: Panichnantakul, Pudchalaluck, Bourgey, Mathieu, Montpetit, Alexandre, Bourque, Guillaume, Riazalhosseini, Yasser
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 01.01.2016
Schlagworte:
Computational Biology - methods
Gene Expression Profiling - methods
Gene Library
Gene Ontology
High-Throughput Nucleotide Sequencing
Humans
Neoplasms - genetics
Neoplasms - pathology
Quality Control
Transcriptome
Tumor Microenvironment - genetics
Next-generation sequencing
Tumor microenvironment
RNA-Seq
Bioinformatics
ISSN:1940-6029, 1940-6029
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Zusammenfassung:The transcriptome is composed of different types of RNA molecules including mRNAs, tRNAs, rRNAs, and other noncoding RNAs that are found inside a cell at a given time. Analyzing transcriptome patterns can shed light on the functional state of the cell as well as on the dynamics of cellular behavior associated with genomic and environmental changes. Likewise, transcriptome analysis has been a major help in solving biological issues and understanding the molecular basis of many diseases including human cancers. Specifically, since targeted and whole genome sequencing studies are becoming more common in identifying the driving factors of cancer, a comprehensive and high-resolution analysis of the transcriptome, as provided by RNA-Sequencing (RNA-Seq), plays a key role in investigating the functional relevance of the identified genomic aberrations. Here, we describe experimental procedures of RNA-Seq and downstream data processing and analysis, with a focus on the identification of abnormally expressed transcripts and genes.
Bibliographie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1940-6029
1940-6029
DOI:10.1007/978-1-4939-3801-8_22