Differential and coherent processing patterns from small RNAs

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Differential and coherent processing patterns from small RNAs. / Pundhir, Sachin; Gorodkin, Jan.

In: Scientific Reports, Vol. 5, 12062, 13.07.2015.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Pundhir, S & Gorodkin, J 2015, 'Differential and coherent processing patterns from small RNAs', Scientific Reports, vol. 5, 12062. https://doi.org/10.1038/srep12062

APA

Pundhir, S., & Gorodkin, J. (2015). Differential and coherent processing patterns from small RNAs. Scientific Reports, 5, [12062]. https://doi.org/10.1038/srep12062

Vancouver

Pundhir S, Gorodkin J. Differential and coherent processing patterns from small RNAs. Scientific Reports. 2015 Jul 13;5. 12062. https://doi.org/10.1038/srep12062

Author

Pundhir, Sachin ; Gorodkin, Jan. / Differential and coherent processing patterns from small RNAs. In: Scientific Reports. 2015 ; Vol. 5.

Bibtex

@article{ef94045aa03649a3bf433bb370a18278,
title = "Differential and coherent processing patterns from small RNAs",
abstract = "Post-transcriptional processing events related to short RNAs are often reflected in their read profile patterns emerging from high-throughput sequencing data. MicroRNA arm switching across different tissues is a well-known example of what we define as differential processing. Here, short RNAs from the nine cell lines of the ENCODE project, irrespective of their annotation status, were analyzed for genomic loci representing differential or coherent processing. We observed differential processing predominantly in RNAs annotated as miRNA, snoRNA or tRNA. Four out of five known cases of differentially processed miRNAs that were in the input dataset were recovered and several novel cases were discovered. In contrast to differential processing, coherent processing is observed widespread in both annotated and unannotated regions. While the annotated loci predominantly consist of ~24nt short RNAs, the unannotated loci comparatively consist of ~17nt short RNAs. Furthermore, these ~17nt short RNAs are significantly enriched for overlap to transcription start sites and DNase I hypersensitive sites (p-value < 0.01) that are characteristic features of transcription initiation RNAs. We discuss how the computational pipeline developed in this study has the potential to be applied to other forms of RNA-seq data for further transcriptome-wide studies of differential and coherent processing.",
author = "Sachin Pundhir and Jan Gorodkin",
year = "2015",
month = jul,
day = "13",
doi = "10.1038/srep12062",
language = "English",
volume = "5",
journal = "Scientific Reports",
issn = "2045-2322",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Differential and coherent processing patterns from small RNAs

AU - Pundhir, Sachin

AU - Gorodkin, Jan

PY - 2015/7/13

Y1 - 2015/7/13

N2 - Post-transcriptional processing events related to short RNAs are often reflected in their read profile patterns emerging from high-throughput sequencing data. MicroRNA arm switching across different tissues is a well-known example of what we define as differential processing. Here, short RNAs from the nine cell lines of the ENCODE project, irrespective of their annotation status, were analyzed for genomic loci representing differential or coherent processing. We observed differential processing predominantly in RNAs annotated as miRNA, snoRNA or tRNA. Four out of five known cases of differentially processed miRNAs that were in the input dataset were recovered and several novel cases were discovered. In contrast to differential processing, coherent processing is observed widespread in both annotated and unannotated regions. While the annotated loci predominantly consist of ~24nt short RNAs, the unannotated loci comparatively consist of ~17nt short RNAs. Furthermore, these ~17nt short RNAs are significantly enriched for overlap to transcription start sites and DNase I hypersensitive sites (p-value < 0.01) that are characteristic features of transcription initiation RNAs. We discuss how the computational pipeline developed in this study has the potential to be applied to other forms of RNA-seq data for further transcriptome-wide studies of differential and coherent processing.

AB - Post-transcriptional processing events related to short RNAs are often reflected in their read profile patterns emerging from high-throughput sequencing data. MicroRNA arm switching across different tissues is a well-known example of what we define as differential processing. Here, short RNAs from the nine cell lines of the ENCODE project, irrespective of their annotation status, were analyzed for genomic loci representing differential or coherent processing. We observed differential processing predominantly in RNAs annotated as miRNA, snoRNA or tRNA. Four out of five known cases of differentially processed miRNAs that were in the input dataset were recovered and several novel cases were discovered. In contrast to differential processing, coherent processing is observed widespread in both annotated and unannotated regions. While the annotated loci predominantly consist of ~24nt short RNAs, the unannotated loci comparatively consist of ~17nt short RNAs. Furthermore, these ~17nt short RNAs are significantly enriched for overlap to transcription start sites and DNase I hypersensitive sites (p-value < 0.01) that are characteristic features of transcription initiation RNAs. We discuss how the computational pipeline developed in this study has the potential to be applied to other forms of RNA-seq data for further transcriptome-wide studies of differential and coherent processing.

U2 - 10.1038/srep12062

DO - 10.1038/srep12062

M3 - Journal article

C2 - 26166713

VL - 5

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 12062

ER -

ID: 143282228