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appreci8: a pipeline for precise variant calling integrating 8 tools

AbstractMotivation. The application of next-generation sequencing in research and particularly in clinical routine requires valid variant calling results. Howe

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Bibliographic Details
Main Authors: Sandmann, Sarah (Author) , Rohde, Christian (Author) , Göllner, Stefanie (Author) , Müller-Tidow, Carsten (Author)
Format: Article (Journal)
Language:English
Published: 26 June 2018
In: Bioinformatics
Year: 2018, Volume: 34, Issue: 24, Pages: 4205-4212
ISSN:1367-4811
DOI:10.1093/bioinformatics/bty518
Online Access:Verlag, Volltext: https://doi.org/10.1093/bioinformatics/bty518
Verlag, Volltext: https://academic.oup.com/bioinformatics/article/34/24/4205/5045348
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Author Notes:Sarah Sandmann, Mohsen Karimi, Aniek O. de Graaf, Christian Rohde, Stefanie Göllner, Julian Varghese, Jan Ernsting, Gunilla Walldin, Bert A. van der Reijden, Carsten Müller-Tidow, Luca Malcovati, Eva Hellström-Lindberg, Joop H. Jansen and Martin Dugas
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Summary:AbstractMotivation. The application of next-generation sequencing in research and particularly in clinical routine requires valid variant calling results. Howe
Item Description:Gesehen am 16.05.2019
Physical Description:Online Resource
ISSN:1367-4811
DOI:10.1093/bioinformatics/bty518

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