View in EDS PDF Full Text

CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.

Saved in:
Bibliographic Details
Title: CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.
Authors: Johansson LF; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands., van Dijk F; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands., de Boer EN; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., van Dijk-Bos KK; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., Jongbloed JD; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., van der Hout AH; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., Westers H; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., Sinke RJ; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., Swertz MA; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands., Sijmons RH; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., Sikkema-Raddatz B; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
Source: Human mutation [Hum Mutat] 2016 May; Vol. 37 (5), pp. 457-64. Date of Electronic Publication: 2016 Feb 24.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 26864275
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Johansson+LF%22">Johansson LF</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Dijk+F%22">van Dijk F</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22de+Boer+EN%22">de Boer EN</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Dijk-Bos+KK%22">van Dijk-Bos KK</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Jongbloed+JD%22">Jongbloed JD</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+der+Hout+AH%22">van der Hout AH</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Westers+H%22">Westers H</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Sinke+RJ%22">Sinke RJ</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Swertz+MA%22">Swertz MA</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Sijmons+RH%22">Sijmons RH</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Sikkema-Raddatz+B%22">Sikkema-Raddatz B</searchLink>; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2016 May; Vol. 37 (5), pp. 457-64. <i>Date of Electronic Publication: </i>2016 Feb 24.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, Non-U.S. Gov't
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1098-1004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597794%22">10597794 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mutat <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26864275
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/humu.22969
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 457
    Titles:
      – TitleFull: CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Johansson LF
      – PersonEntity:
          Name:
            NameFull: van Dijk F
      – PersonEntity:
          Name:
            NameFull: de Boer EN
      – PersonEntity:
          Name:
            NameFull: van Dijk-Bos KK
      – PersonEntity:
          Name:
            NameFull: Jongbloed JD
      – PersonEntity:
          Name:
            NameFull: van der Hout AH
      – PersonEntity:
          Name:
            NameFull: Westers H
      – PersonEntity:
          Name:
            NameFull: Sinke RJ
      – PersonEntity:
          Name:
            NameFull: Swertz MA
      – PersonEntity:
          Name:
            NameFull: Sijmons RH
      – PersonEntity:
          Name:
            NameFull: Sikkema-Raddatz B
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 05
              Text: 2016 May
              Type: published
              Y: 2016
          Identifiers:
            – Type: issn-electronic
              Value: 1098-1004
          Numbering:
            – Type: volume
              Value: 37
            – Type: issue
              Value: 5
          Titles:
            – TitleFull: Human mutation
              Type: main
ResultId 1