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Learn MoreNext-generation sequencing (NGS) has revolutionized systems-based analysis of cellular pathways. The goals of this study are to compare NGS-derived human M1- and M2-like macrophage profiling (RNA-seq) to microarray and quantitative reverse transcription polymerase chain reaction (qRTPCR) methods and to establish a high resolution transcriptome of human macrophages.; Total RNA was isolated from classically and aternative activated human macrophages.mRNA profiles were generated by deep sequencing og M1 and M2 macrophages from 3 donors using Illumina HiSeqSQ. The sequence reads that passed quality filters were analyzed at the transcript isoform level with two methods: Casava1.8 and TopHat followed by Cufflinks. qRTPCR validation was performed using LightCycler and SYBR Green assays. SOURCE: Andrea Nino Castro (anino@uni-bonn.de) - Genomics and Immunoregulation Life and Medical Sciences institute
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