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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
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We are analyzing https://link.springer.com/article/10.1186/s13059-014-0491-2.

Title:
Genome-wide profiling of mouse RNA secondary structures reveals key features of the mammalian transcriptome | Genome Biology
Description:
Background The understanding of RNA structure is a key feature toward the comprehension of RNA functions and mechanisms of action. In particular, non-coding RNAs are thought to exert their functions by specific secondary structures, but an efficient annotation on a large scale of these structures is still missing. Results By using a novel high-throughput method, named chemical inference of RNA structures, CIRS-seq, that uses dimethyl sulfate, and N-cyclohexyl- N
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Books & Literature

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,626,432 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

While many websites aim to make money, others are created to share knowledge or showcase creativity. People build websites for various reasons. This could be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

rna, pubmed, article, google, scholar, structure, structures, cirsseq, reactivity, secondary, analysis, data, central, rnas, structural, figure, average, folding, regions, file, mouse, transcripts, biol, coding, additional, nucleotides, cell, noncoding, lina, binding, human, chemical, mrnas, region, protein, cells, methods, utr, method, native, ncrnas, probing, dms, mol, conformation, vivo, test, authors, higher, escs,

Topics {✒️}

cirs-seq-guided folding outperformed cirs-seq-derived data compared superimposed dms/shape-reactive positions perform transcriptome-wide probing cirs-seq methodology represents cirs-seq constrained structures cirs-seq data correlated cirs-seq data improves de novo prediction full size image cirs-seq-derived structures superimposed dms/cmct-reactive positions cirs-seq data revealed superimposed shape-reactive positions vivo genome-wide profiling obtain genome-wide information integrates single-nucleotide variants internal loop il2/il2′ n-cyclohexyl-n'-beta rna-seq library preparation article download pdf carbodiimide metho-p-toluenesulfonate canonical rna-seq data g-rich dna flap protein-facilitated rna folding genome-wide profiling embryonic stem cells stem-loop structure located single-stranded rna residues mouse protein-coding transcripts secondary structure inferred related subjects u5 tri-snrnp particles yeast spliceosomal u4/u6 low-abundance u12 snrna probe protein-coding rnas protein-coding rnas revealed sample secondary structures modification-induced reverse transcription low-abundance u12 snrnas cirs-seq data genome-wide measurement genome-wide probing full access rna-seq data recently published variant pomeranz krummel da teulade-fichou m shape data files dms/cmct treatment induced

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Genome-wide profiling of mouse RNA secondary structures reveals key features of the mammalian transcriptome
         description:The understanding of RNA structure is a key feature toward the comprehension of RNA functions and mechanisms of action. In particular, non-coding RNAs are thought to exert their functions by specific secondary structures, but an efficient annotation on a large scale of these structures is still missing. By using a novel high-throughput method, named chemical inference of RNA structures, CIRS-seq, that uses dimethyl sulfate, and N-cyclohexyl- N'-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate to modify RNA residues in single-stranded conformation within native deproteinized RNA secondary structures, we investigate the structural features of mouse embryonic stem cell transcripts. Our analysis reveals an unexpected higher structuring of the 5′ and 3′ untranslated regions compared to the coding regions, a reduced structuring at the Kozak sequence and stop codon, and a three-nucleotide periodicity across the coding region of messenger RNAs. We also observe that ncRNAs exhibit a higher degree of structuring with respect to protein coding transcripts. Moreover, we find that the Lin28a binding protein binds selectively to RNA motifs with a strong preference toward a single stranded conformation. This work defines for the first time the complete RNA structurome of mouse embryonic stem cells, revealing an extremely distinct RNA structural landscape. These results demonstrate that CIRS-seq constitutes an important tool for the identification of native deproteinized RNA structures.
         datePublished:2014-10-17T00:00:00Z
         dateModified:2014-10-17T00:00:00Z
         pageStart:1
         pageEnd:13
         license:http://creativecommons.org/licenses/by/4.0/
         sameAs:https://doi.org/10.1186/s13059-014-0491-2
         keywords:
            Positive Predictive Value
            Mouse Embryonic Stem Cell
            Mouse ESCs
            Kozak Sequence
            Normalize Read Count
            Animal Genetics and Genomics
            Human Genetics
            Plant Genetics and Genomics
            Microbial Genetics and Genomics
            Bioinformatics
            Evolutionary Biology
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         isPartOf:
            name:Genome Biology
            issn:
               1474-760X
            volumeNumber:15
            type:
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            name:BioMed Central
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         author:
               name:Danny Incarnato
               affiliation:
                     name:Human Genetics Foundation (HuGeF)
                     address:
                        name:Human Genetics Foundation (HuGeF), Torino, Italy
                        type:PostalAddress
                     type:Organization
                     name:Università di Siena
                     address:
                        name:Dipartimento di Biotecnologie Chimica e Farmacia, Università di Siena, Siena, Italy
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               name:Francesco Neri
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                     address:
                        name:Human Genetics Foundation (HuGeF), Torino, Italy
                        type:PostalAddress
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               name:Francesca Anselmi
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                     address:
                        name:Human Genetics Foundation (HuGeF), Torino, Italy
                        type:PostalAddress
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               name:Salvatore Oliviero
               affiliation:
                     name:Human Genetics Foundation (HuGeF)
                     address:
                        name:Human Genetics Foundation (HuGeF), Torino, Italy
                        type:PostalAddress
                     type:Organization
                     name:Università di Torino
                     address:
                        name:Dipartimento di Scienze della Vita e Biologia dei Sistemi, Università di Torino, Torino, Italy
                        type:PostalAddress
                     type:Organization
               email:[email protected]
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         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Genome-wide profiling of mouse RNA secondary structures reveals key features of the mammalian transcriptome
      description:The understanding of RNA structure is a key feature toward the comprehension of RNA functions and mechanisms of action. In particular, non-coding RNAs are thought to exert their functions by specific secondary structures, but an efficient annotation on a large scale of these structures is still missing. By using a novel high-throughput method, named chemical inference of RNA structures, CIRS-seq, that uses dimethyl sulfate, and N-cyclohexyl- N'-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate to modify RNA residues in single-stranded conformation within native deproteinized RNA secondary structures, we investigate the structural features of mouse embryonic stem cell transcripts. Our analysis reveals an unexpected higher structuring of the 5′ and 3′ untranslated regions compared to the coding regions, a reduced structuring at the Kozak sequence and stop codon, and a three-nucleotide periodicity across the coding region of messenger RNAs. We also observe that ncRNAs exhibit a higher degree of structuring with respect to protein coding transcripts. Moreover, we find that the Lin28a binding protein binds selectively to RNA motifs with a strong preference toward a single stranded conformation. This work defines for the first time the complete RNA structurome of mouse embryonic stem cells, revealing an extremely distinct RNA structural landscape. These results demonstrate that CIRS-seq constitutes an important tool for the identification of native deproteinized RNA structures.
      datePublished:2014-10-17T00:00:00Z
      dateModified:2014-10-17T00:00:00Z
      pageStart:1
      pageEnd:13
      license:http://creativecommons.org/licenses/by/4.0/
      sameAs:https://doi.org/10.1186/s13059-014-0491-2
      keywords:
         Positive Predictive Value
         Mouse Embryonic Stem Cell
         Mouse ESCs
         Kozak Sequence
         Normalize Read Count
         Animal Genetics and Genomics
         Human Genetics
         Plant Genetics and Genomics
         Microbial Genetics and Genomics
         Bioinformatics
         Evolutionary Biology
      image:
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         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13059-014-0491-2/MediaObjects/13059_2014_Article_491_Fig3_HTML.jpg
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13059-014-0491-2/MediaObjects/13059_2014_Article_491_Fig4_HTML.jpg
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13059-014-0491-2/MediaObjects/13059_2014_Article_491_Fig5_HTML.jpg
      isPartOf:
         name:Genome Biology
         issn:
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         name:BioMed Central
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            name:Danny Incarnato
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                  address:
                     name:Human Genetics Foundation (HuGeF), Torino, Italy
                     type:PostalAddress
                  type:Organization
                  name:Università di Siena
                  address:
                     name:Dipartimento di Biotecnologie Chimica e Farmacia, Università di Siena, Siena, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Francesco Neri
            affiliation:
                  name:Human Genetics Foundation (HuGeF)
                  address:
                     name:Human Genetics Foundation (HuGeF), Torino, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Francesca Anselmi
            affiliation:
                  name:Human Genetics Foundation (HuGeF)
                  address:
                     name:Human Genetics Foundation (HuGeF), Torino, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Salvatore Oliviero
            affiliation:
                  name:Human Genetics Foundation (HuGeF)
                  address:
                     name:Human Genetics Foundation (HuGeF), Torino, Italy
                     type:PostalAddress
                  type:Organization
                  name:Università di Torino
                  address:
                     name:Dipartimento di Scienze della Vita e Biologia dei Sistemi, Università di Torino, Torino, Italy
                     type:PostalAddress
                  type:Organization
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            address:
               name:Human Genetics Foundation (HuGeF), Torino, Italy
               type:PostalAddress
            type:Organization
            name:Università di Siena
            address:
               name:Dipartimento di Biotecnologie Chimica e Farmacia, Università di Siena, Siena, Italy
               type:PostalAddress
            type:Organization
      name:Francesco Neri
      affiliation:
            name:Human Genetics Foundation (HuGeF)
            address:
               name:Human Genetics Foundation (HuGeF), Torino, Italy
               type:PostalAddress
            type:Organization
      name:Francesca Anselmi
      affiliation:
            name:Human Genetics Foundation (HuGeF)
            address:
               name:Human Genetics Foundation (HuGeF), Torino, Italy
               type:PostalAddress
            type:Organization
      name:Salvatore Oliviero
      affiliation:
            name:Human Genetics Foundation (HuGeF)
            address:
               name:Human Genetics Foundation (HuGeF), Torino, Italy
               type:PostalAddress
            type:Organization
            name:Università di Torino
            address:
               name:Dipartimento di Scienze della Vita e Biologia dei Sistemi, Università di Torino, Torino, Italy
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Human Genetics Foundation (HuGeF), Torino, Italy
      name:Dipartimento di Biotecnologie Chimica e Farmacia, Università di Siena, Siena, Italy
      name:Human Genetics Foundation (HuGeF), Torino, Italy
      name:Human Genetics Foundation (HuGeF), Torino, Italy
      name:Human Genetics Foundation (HuGeF), Torino, Italy
      name:Dipartimento di Scienze della Vita e Biologia dei Sistemi, Università di Torino, Torino, Italy

External Links {🔗}(277)

Analytics and Tracking {📊}

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Libraries {📚}

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