https://doi.org/10.7490/f1000research.1116095.1
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Giurgiu M, Scharf F, Arnold A et al. Development of a low-frequency variant calling tool for the analysis of tumor samples processed with ultra-deep next-generation sequencing [version 1; not peer reviewed]. F1000Research 2018, 7:1480 (poster) (https://doi.org/10.7490/f1000research.1116095.1)
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Development of a low-frequency variant calling tool for the analysis of tumor samples processed with ultra-deep next-generation sequencing

Madalina Giurgiu1, Florentine Scharf, Anke Arnold, Andreas Laner, Julia Romic-Pickl, Anna Benet-Pages, Elke Holinski-Feder
Author Affiliations
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Published 17 Sep 2018

Development of a low-frequency variant calling tool for the analysis of tumor samples processed with ultra-deep next-generation sequencing

[version 1; not peer reviewed]

Madalina Giurgiu1, Florentine Scharf, Anke Arnold, Andreas Laner, Julia Romic-Pickl, Anna Benet-Pages, Elke Holinski-Feder
Author Affiliations
1 Medical Genetics Center Munich, Germany
Presented at
Genome Informatics 2018
Abstract
Competing Interests

No competing interests were disclosed

Keywords
LowFreq, ultra-deep NGS, low-frequency variants, tumor
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