View in EDS HTML Full Text PDF Full Text

GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss.

Saved in:
Bibliographic Details
Title: GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss.
Authors: Melidis DP; L3S Research Center, Leibniz University Hannover, Hannover, Germany., Landgraf C; Department of Human Genetics, Hannover Medical School, Hannover, Germany., Schmidt G; Department of Human Genetics, Hannover Medical School, Hannover, Germany., Schöner-Heinisch A; Department of Human Genetics, Hannover Medical School, Hannover, Germany., von Hardenberg S; Department of Human Genetics, Hannover Medical School, Hannover, Germany., Lesinski-Schiedat A; Department of Otorhinolaryngology, Hannover Medical School, Hannover, Germany.; Hearing4all Cluster of Excellence, Hannover Medical School, Hannover, Germany., Nejdl W; L3S Research Center, Leibniz University Hannover, Hannover, Germany.; Knowledge-based Systems Laboratory, Leibniz University Hannover, Hannover, Germany., Auber B; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Source: PLoS computational biology [PLoS Comput Biol] 2022 Sep 21; Vol. 18 (9), pp. e1009785. Date of Electronic Publication: 2022 Sep 21 (Print Publication: 2022).
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101238922 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7358 (Electronic) Linking ISSN: 1553734X NLM ISO Abbreviation: PLoS Comput Biol Subsets: MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 36129964
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Melidis+DP%22">Melidis DP</searchLink>; L3S Research Center, Leibniz University Hannover, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Landgraf+C%22">Landgraf C</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Schmidt+G%22">Schmidt G</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Schöner-Heinisch+A%22">Schöner-Heinisch A</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22von+Hardenberg+S%22">von Hardenberg S</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Lesinski-Schiedat+A%22">Lesinski-Schiedat A</searchLink>; Department of Otorhinolaryngology, Hannover Medical School, Hannover, Germany.; Hearing4all Cluster of Excellence, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Nejdl+W%22">Nejdl W</searchLink>; L3S Research Center, Leibniz University Hannover, Hannover, Germany.; Knowledge-based Systems Laboratory, Leibniz University Hannover, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Auber+B%22">Auber B</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101238922%22">PLoS computational biology</searchLink> [PLoS Comput Biol] 2022 Sep 21; Vol. 18 (9), pp. e1009785. <i>Date of Electronic Publication: </i>2022 Sep 21 (<i>Print Publication: </i>2022).
– 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="%22Public+Library+of+Science%22">Public Library of Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101238922 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1553-7358 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%221553734X%22">1553734X </searchLink><i>NLM ISO Abbreviation: </i>PLoS Comput Biol <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=36129964
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1371/journal.pcbi.1009785
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: e1009785
    Titles:
      – TitleFull: GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Melidis DP
      – PersonEntity:
          Name:
            NameFull: Landgraf C
      – PersonEntity:
          Name:
            NameFull: Schmidt G
      – PersonEntity:
          Name:
            NameFull: Schöner-Heinisch A
      – PersonEntity:
          Name:
            NameFull: von Hardenberg S
      – PersonEntity:
          Name:
            NameFull: Lesinski-Schiedat A
      – PersonEntity:
          Name:
            NameFull: Nejdl W
      – PersonEntity:
          Name:
            NameFull: Auber B
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 21
              M: 09
              Text: 2022 Sep 21
              Type: published
              Y: 2022
          Identifiers:
            – Type: issn-electronic
              Value: 1553-7358
          Numbering:
            – Type: volume
              Value: 18
            – Type: issue
              Value: 9
          Titles:
            – TitleFull: PLoS computational biology
              Type: main
ResultId 1