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Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data

Cancer cell lines (CCL) are an integral part of modern cancer research but are susceptible to misidentification. The increasing popularity of sequencing technologies motivates the in-silico identification of CCLs based on their mutational fingerprint, but care must be taken when identifying heteroge...

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Autores principales: Otto, Raik, Rössler, Jan-Niklas, Sers, Christine, Mamlouk, Soulafa, Leser, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344579/
https://www.ncbi.nlm.nih.gov/pubmed/30674903
http://dx.doi.org/10.1038/s41598-018-36300-8
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author Otto, Raik
Rössler, Jan-Niklas
Sers, Christine
Mamlouk, Soulafa
Leser, Ulf
author_facet Otto, Raik
Rössler, Jan-Niklas
Sers, Christine
Mamlouk, Soulafa
Leser, Ulf
author_sort Otto, Raik
collection PubMed
description Cancer cell lines (CCL) are an integral part of modern cancer research but are susceptible to misidentification. The increasing popularity of sequencing technologies motivates the in-silico identification of CCLs based on their mutational fingerprint, but care must be taken when identifying heterogeneous data. We recently developed the proof-of-concept Uniquorn 1 method which could reliably identify heterogeneous sequencing data from selected sequencing technologies. Here we present Uniquorn 2, a generic and robust in-silico identification method for CCLs with DNA/RNA-seq and panel-seq information. We benchmarked Uniquorn 2 by cross-identifying 1612 RNA and 3596 panel-sized NGS profiles derived from 1516 CCLs, five repositories, four technologies and three major cancer panel-designs. Our method achieves an accuracy of 96% for RNA-seq and 95% for mixed DNA-seq and RNA-seq identification. Even for a panel of only 94 cancer-related genes, accuracy remains at 82% but decreases when using smaller panels. Uniquorn 2 is freely available as R-Bioconductor-package ‘Uniquorn’.
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spelling pubmed-63445792019-01-28 Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data Otto, Raik Rössler, Jan-Niklas Sers, Christine Mamlouk, Soulafa Leser, Ulf Sci Rep Article Cancer cell lines (CCL) are an integral part of modern cancer research but are susceptible to misidentification. The increasing popularity of sequencing technologies motivates the in-silico identification of CCLs based on their mutational fingerprint, but care must be taken when identifying heterogeneous data. We recently developed the proof-of-concept Uniquorn 1 method which could reliably identify heterogeneous sequencing data from selected sequencing technologies. Here we present Uniquorn 2, a generic and robust in-silico identification method for CCLs with DNA/RNA-seq and panel-seq information. We benchmarked Uniquorn 2 by cross-identifying 1612 RNA and 3596 panel-sized NGS profiles derived from 1516 CCLs, five repositories, four technologies and three major cancer panel-designs. Our method achieves an accuracy of 96% for RNA-seq and 95% for mixed DNA-seq and RNA-seq identification. Even for a panel of only 94 cancer-related genes, accuracy remains at 82% but decreases when using smaller panels. Uniquorn 2 is freely available as R-Bioconductor-package ‘Uniquorn’. Nature Publishing Group UK 2019-01-23 /pmc/articles/PMC6344579/ /pubmed/30674903 http://dx.doi.org/10.1038/s41598-018-36300-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Otto, Raik
Rössler, Jan-Niklas
Sers, Christine
Mamlouk, Soulafa
Leser, Ulf
Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data
title Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data
title_full Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data
title_fullStr Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data
title_full_unstemmed Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data
title_short Robust in-silico identification of Cancer Cell Lines based on RNA and targeted DNA sequencing data
title_sort robust in-silico identification of cancer cell lines based on rna and targeted dna sequencing data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344579/
https://www.ncbi.nlm.nih.gov/pubmed/30674903
http://dx.doi.org/10.1038/s41598-018-36300-8
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