<p>A comprehensive benchmark of somatic CNV calling tools on short-read WGS and WES data</p>

Ana Popic; Vladimir Tomic; Vojiislav  Varjacic; Ariella  Sasson; Sujaya  Srinivasan; Jelena  Ranđelović; Svetozar  Nešić

doi:10.7490/f1000research.1117435.1

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Popic A, Tomic V, Varjacic V et al. A comprehensive benchmark of somatic CNV calling tools on short-read WGS and WES data [version 1; not peer reviewed]. F1000Research 2019, 8(ISCB Comm J):1552 (poster) (https://doi.org/10.7490/f1000research.1117435.1)

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A comprehensive benchmark of somatic CNV calling tools on short-read WGS and WES data

Ana Popic¹, Vladimir Tomic¹, Vojiislav Varjacic¹, Ariella Sasson, Sujaya Srinivasan, Jelena Ranđelović, Svetozar Nešić

Published 30 Aug 2019 (https://doi.org/10.7490/f1000research.1117435.1)

Author Affiliations

¹ Seven Bridges, Serbia

Copyright © 2019 Popic A et al. This is an open access work distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Published 30 Aug 2019

A comprehensive benchmark of somatic CNV calling tools on short-read WGS and WES data
[version 1; not peer reviewed]

Ana Popic¹, Vladimir Tomic¹, Vojiislav Varjacic¹, Ariella Sasson, Sujaya Srinivasan, Jelena Ranđelović, Svetozar Nešić

Author Affiliations

¹ Seven Bridges, Serbia

Presented at

ISMB/ECCB 2019

Abstract

Competing Interests

No competing interests were disclosed

Keywords

copy number variation, evaluation studies, whole-exome sequencing, whole-genome sequencing, consensus calling, rabix, common workflow language

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