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Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Long non-coding RNA landscape in human monocytes

ABSTRACT: We report the lncRNAs transcribed in the human primary monocyte cells. We performed deep RNA sequencing from four healthy individuals. In addition, the raw RNA-Seq data from 11 human monocyte samples were selected from public databases and generated a total ~1.7 billion reads. We identified ~ 8,000 lncRNAs from all the datasets of which more than 1,000 of them have not been previously reported in monocytes. We also validated a few of these novel lncRNAs in monocytes and other hematopoetic cell types. The other 11 datasets were taken from the following: ENCSR000CUC 6 samples E-MTAB-2399 4 samples GSM1526678 mRNA profiling of monocytes cells from 4 healthy individuals

ORGANISM(S): Homo sapiens

SUBMITTER: Srikanth Manda

PROVIDER: E-GEOD-69753 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Long non-coding RNA expression in primary human monocytes.

Mirsafian Hoda H Manda Srinivas Srikanth SS Mitchell Christopher J CJ Sreenivasamurthy Sreelakshmi S Ripen Adiratna Mat AM Mohamad Saharuddin Bin SB Merican Amir Feisal AF Pandey Akhilesh A

Genomics 20160108 1

Long non-coding RNAs (lncRNAs) have been shown to possess a wide range of functions in both cellular and developmental processes including cancers. Although some of the lncRNAs have been implicated in the regulation of the immune response, the exact function of the large majority of lncRNAs still remains unknown. In this study, we characterized the lncRNAs in human primary monocytes, an essential component of the innate immune system. We performed RNA sequencing of monocytes from four individual ...[more]

PMID: 26778813

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Long non-coding RNA landscape in human monocytes

Project description:We report the lncRNAs transcribed in the human primary monocyte cells. We performed deep RNA sequencing from four healthy individuals. In addition, the raw RNA-Seq data from 11 human monocyte samples were selected from public databases and generated a total ~1.7 billion reads. We identified ~ 8,000 lncRNAs from all the datasets of which more than 1,000 of them have not been previously reported in monocytes. We also validated a few of these novel lncRNAs in monocytes and other hematopoetic cell types. The other 11 datasets were taken from the following: ENCSR000CUC 6 samples E-MTAB-2399 4 samples GSM1526678

2016-02-19 | GSE69753 | GEO

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2014-05-02 | E-GEOD-54401 | biostudies-arrayexpress

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Project description:Monocytes play a central role in the inflammatory response that follows acute myocardial infarction (MI). In order to study phenotypic adaptation of this cell type, we investigated patterns of monocyte gene expression in circulating monocytes at various stages of MI. Circulating monocytes were isolated from venous blood of MI patients at three time points: t1: within 6 hours after onset of chest pain (acute phase), t2: 3 days after MI (subacute phase), t3: 90 days after MI (chronic phase). For comparison, we studied a control group (n=21, data to be submitted later) with stable coronary artery disease. Using this transcriptomic analysis, we aimed to provide a more comprehensive reference of monocyte biology following acute MI and to aid in the identification of novel pathways and genes influencing the course of MI. Monocytes play a central role in the inflammatory response that follows acute myocardial infarction (MI). In order to study phenotypic adaptation of this cell type, we investigated patterns of monocyte gene expression in circulating monocytes at various stages of MI. Circulating monocytes were isolated from venous blood of MI patients at three time points: t1: within 6 hours after onset of chest pain (acute phase), t2: 3 days after MI (subacute phase), t3: 90 days after MI (chronic phase). For comparison, we studied a control group (n=21, data to be submitted later) with stable coronary artery disease. Illumina Ref-8 v3.0 microarray arrays were used for whole-genome transcriptional profiling.

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