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10.1007/s00335-015-9593-8

http://scihub22266oqcxt.onion/10.1007/s00335-015-9593-8
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suck abstract from ncbi


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pmid26253466
      Mamm+Genome 2015 ; 26 (9-10 ): 391-402
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  • Paradigm shifts in genomics through the FANTOM projects #MMPMID26253466
  • de Hoon M ; Shin JW ; Carninci P
  • Mamm Genome 2015[Oct]; 26 (9-10 ): 391-402 PMID26253466 show ga
  • Big leaps in science happen when scientists from different backgrounds interact. In the past 15 years, the FANTOM Consortium has brought together scientists from different fields to analyze and interpret genomic data produced with novel technologies, including mouse full-length cDNAs and, more recently, expression profiling at single-nucleotide resolution by cap-analysis gene expression. The FANTOM Consortium has provided the most comprehensive mouse cDNA collection for functional studies and extensive maps of the human and mouse transcriptome comprising promoters, enhancers, as well as the network of their regulatory interactions. More importantly, serendipitous observations of the FANTOM dataset led us to realize that the mammalian genome is pervasively transcribed, even from retrotransposon elements, which were previously considered junk DNA. The majority of products from the mammalian genome are long non-coding RNAs (lncRNAs), including sense-antisense, intergenic, and enhancer RNAs. While the biological function has been elucidated for some lncRNAs, more than 98 % of them remain without a known function. We argue that large-scale studies are urgently needed to address the functional role of lncRNAs.
  • |*Gene Expression Profiling [MESH]
  • |*Genomics [MESH]
  • |Animals [MESH]
  • |DNA, Complementary/genetics [MESH]
  • |Genome [MESH]
  • |Humans [MESH]
  • |Mice [MESH]
  • |Promoter Regions, Genetic [MESH]
  • |RNA, Long Noncoding/*genetics [MESH]
  • |Regulatory Sequences, Nucleic Acid/genetics [MESH]


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