Author

Paul C Boutros

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:long-read sequencing· 1 Research Focus:software / tool· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Jared T Simpson· 2 shared Akihiro FujimotoiD· 1 shared Ali Bashashati· 1 shared Andrew G Lynch· 1 shared Anne-Sophie Sertier· 1 shared Barbara HutteriD· 1 shared Benedikt BrorsiD· 1 shared Bruno Grande· 1 shared

Activity by Year

2015-2016 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersBioinformatics

Jared T Simpson

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Nanocall: An Open Source Basecaller for Oxford Nanopore Sequencing Data

Matei David, Lewis Jonathan Dursi, Delia Yao, Paul C Boutros, Jared T Simpson

Nanocall is an open-source basecaller for Oxford Nanopore sequencing data that enables offline analysis and has comparable accuracy to Metrichor's cloud-based solution.

bioRxiv · Mar 28, 2016Bioinformatics

Kronos: a workflow assembler for genome analytics and informatics

M Jafar Taghiyar, Jamie Rosner, Diljot Grewal, Bruno Grande, Radhouane Aniba, Jasleen Grewal, Paul C Boutros, Ryan D Morin, Ali Bashashati, Sohrab P Shah

Kronos automates bioinformatics workflow development and execution, enabling reproducible and distributable analysis of NGS datasets through configuration-based Python applications.

bioRxiv · Feb 22, 2016Bioinformatics

A Comprehensive Assessment of Somatic Mutation Calling in Cancer Genomes

Tyler S Alioto, Sophia Derdak, Timothy A Beck, Paul C Boutros, Lawrence Bower, Ivo Buchhalter, Matthew D Eldridge, Nicholas J Harding, Lawrence Edward Heisler, Eivind Hovig, David T W Jones, Andrew G Lynch, Sigve Nakken, Paolo Ribeca, Anne-Sophie Sertier, , Rolf Kab

This study benchmarks somatic mutation calling in cancer genomes, identifying inconsistencies and proposing solutions to improve accuracy.

Nature Communications · Dec 9, 2015Peer-reviewedGenomics