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An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates
Antisense transcription is pervasive among biological systems and one of the products of antisense transcription is natural antisense transcripts (NATs). Emerging evidences suggest that they are key regulators of gene expression. With the discovery of NATs in Plasmodium falciparum, it has been sugge...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536056/ https://www.ncbi.nlm.nih.gov/pubmed/26484136 http://dx.doi.org/10.1016/j.gdata.2014.10.010 |
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author | Subudhi, Amit Kumar Boopathi, P.A. Garg, Shilpi Middha, Sheetal Acharya, Jyoti Pakalapati, Deepak Saxena, Vishal Aiyaz, Mohammed Orekondy, Harsha B. Mugasimangalam, Raja C. Sirohi, Paramendra Kochar, Sanjay K. Kochar, Dhanpat K. Das, Ashis |
author_facet | Subudhi, Amit Kumar Boopathi, P.A. Garg, Shilpi Middha, Sheetal Acharya, Jyoti Pakalapati, Deepak Saxena, Vishal Aiyaz, Mohammed Orekondy, Harsha B. Mugasimangalam, Raja C. Sirohi, Paramendra Kochar, Sanjay K. Kochar, Dhanpat K. Das, Ashis |
author_sort | Subudhi, Amit Kumar |
collection | PubMed |
description | Antisense transcription is pervasive among biological systems and one of the products of antisense transcription is natural antisense transcripts (NATs). Emerging evidences suggest that they are key regulators of gene expression. With the discovery of NATs in Plasmodium falciparum, it has been suggested that these might also be playing regulatory roles in this parasite. However, all the reports describing the diversity of NATs have come from parasites in culture condition except for a recent study published by us. In order to explore the in vivo diversity of NATs in P. falciparum clinical isolates, we performed a whole genome expression profiling using a strand-specific 244 K microarray that contains probes for both sense and antisense transcripts. In this report, we describe the experimental procedure and analysis thereof of the microarray data published recently in Gene Expression Omnibus (GEO) under accession number GSE44921. This published data provide a wealth of information about the prevalence of NATs in P. falciparum clinical isolates from patients with diverse malaria related disease conditions. Supplementary information about the description and interpretation of the data can be found in a recent publication by Subudhi et al. in Experimental Parasitology (2014). |
format | Online Article Text |
id | pubmed-4536056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-45360562015-10-19 An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates Subudhi, Amit Kumar Boopathi, P.A. Garg, Shilpi Middha, Sheetal Acharya, Jyoti Pakalapati, Deepak Saxena, Vishal Aiyaz, Mohammed Orekondy, Harsha B. Mugasimangalam, Raja C. Sirohi, Paramendra Kochar, Sanjay K. Kochar, Dhanpat K. Das, Ashis Genom Data Data in Brief Antisense transcription is pervasive among biological systems and one of the products of antisense transcription is natural antisense transcripts (NATs). Emerging evidences suggest that they are key regulators of gene expression. With the discovery of NATs in Plasmodium falciparum, it has been suggested that these might also be playing regulatory roles in this parasite. However, all the reports describing the diversity of NATs have come from parasites in culture condition except for a recent study published by us. In order to explore the in vivo diversity of NATs in P. falciparum clinical isolates, we performed a whole genome expression profiling using a strand-specific 244 K microarray that contains probes for both sense and antisense transcripts. In this report, we describe the experimental procedure and analysis thereof of the microarray data published recently in Gene Expression Omnibus (GEO) under accession number GSE44921. This published data provide a wealth of information about the prevalence of NATs in P. falciparum clinical isolates from patients with diverse malaria related disease conditions. Supplementary information about the description and interpretation of the data can be found in a recent publication by Subudhi et al. in Experimental Parasitology (2014). Elsevier 2014-10-29 /pmc/articles/PMC4536056/ /pubmed/26484136 http://dx.doi.org/10.1016/j.gdata.2014.10.010 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Data in Brief Subudhi, Amit Kumar Boopathi, P.A. Garg, Shilpi Middha, Sheetal Acharya, Jyoti Pakalapati, Deepak Saxena, Vishal Aiyaz, Mohammed Orekondy, Harsha B. Mugasimangalam, Raja C. Sirohi, Paramendra Kochar, Sanjay K. Kochar, Dhanpat K. Das, Ashis An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates |
title | An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates |
title_full | An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates |
title_fullStr | An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates |
title_full_unstemmed | An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates |
title_short | An in vivo transcriptome data set of natural antisense transcripts from Plasmodium falciparum clinical isolates |
title_sort | in vivo transcriptome data set of natural antisense transcripts from plasmodium falciparum clinical isolates |
topic | Data in Brief |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536056/ https://www.ncbi.nlm.nih.gov/pubmed/26484136 http://dx.doi.org/10.1016/j.gdata.2014.10.010 |
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