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Transposable elements reveal a stem cell-specific class of long noncoding RNAs.

David Kelley | John Rinn
Genome biology | 2012

Numerous studies over the past decade have elucidated a large set of long intergenic noncoding RNAs (lincRNAs) in the human genome. Research since has shown that lincRNAs constitute an important layer of genome regulation across a wide spectrum of species. However, the factors governing their evolution and origins remain relatively unexplored. One possible factor driving lincRNA evolution and biological function is transposable element (TE) insertions. Here, we comprehensively characterize the TE content of lincRNAs relative to genomic averages and protein coding transcripts.

Pubmed ID: 23181609

Research resources used in this publication

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Associated grants

  • Agency: NIH HHS, United States
    Id: DP2 OD006670
  • Agency: NIGMS NIH HHS, United States
    Id: P01 GM099117
  • Agency: NHGRI NIH HHS, United States
    Id: P50 HG006193-01
  • Agency: NIH HHS, United States
    Id: DP2OD006670
  • Agency: NHLBI NIH HHS, United States
    Id: T32HL007893

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This is a list of tools and resources that we have found mentioned in this publication.


RepeatMasker (tool)

RRID:SCR_012954

Software tool that screens DNA sequences for interspersed repeats and low complexity DNA sequences. The output of the program is a detailed annotation of the repeats that are present in the query sequence as well as a modified version of the query sequence in which all the annotated repeats have been masked (default: replaced by Ns). Currently over 56% of human genomic sequence is identified and masked by the program. Sequence comparisons in RepeatMasker are performed by one of several popular search engines including nhmmer, cross_match, ABBlast/WUBlast, RMBlast and Decypher. RepeatMasker makes use of curated libraries of repeats and currently supports Dfam ( profile HMM library ) and RepBase ( consensus sequence library ).

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Bowtie (tool)

RRID:SCR_005476

Software ultrafast memory efficient tool for aligning sequencing reads. Bowtie is short read aligner.

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GENCODE (tool)

RRID:SCR_014966

Human and mouse genome annotation project which aims to identify all gene features in the human genome using computational analysis, manual annotation, and experimental validation.

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