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Sander Bollen

dblp:145/5220 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2017
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Systems, architecture and hardware · 1Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › cancer genomics
chromosomal aberration detection
0.212014
CAFE: an R package for the detection of gross chromosomal abnormalities from gene expression microarray data · Bioinform. 2014
Bioinformatics and computational biology › gene expression analysis › microarray data analysis
microarray gene expression analysis
0.212014
CAFE: an R package for the detection of gross chromosomal abnormalities from gene expression microarray data · Bioinform. 2014

Methods — techniques the papers use, named apart from their topics

visualization · 0.2
YearPublicationVenuePosition
2017 BIOPET: towards Scalable, Maintainable, User-friendly, Robust and Flexible NGS data analysis pipelines
abstract
Because of the rapid decreasing of sequencing cost, more research and clinical institutes are generating Next Generation Sequencing data at an increasing and impressive scale. University Medical Centers in the Netherlands are sequencing thousands patients a year each as part of their routine diagnosis. On the research front, the GoNL project and BIOS project coordinated by the BBMRI-NL consortium have sequenced 770 whole genome DNA samples and over 4000 RNA samples collected from a number of Dutch biobanks. In 2016, the deployment of Illumina X Ten sequencer at the Hartwig Medical Foundation provides a sequencing capacity of 18,000 whole genome DNA samples per year. Processing these petabyte scale datasets requires revolutionary thinking and solutions in the computing and storage infrastructure and the data analysis pipelines. At Leiden University Medical Center, we have developed a GATK-Queue based open source pipeline framework - BIOPET (Bioinformatics Pipeline Execution Toolkit). We implemented all our commonly used NGS tools as Queue modules in the form of Scala classes. Together with those that are already supported in GATKQueue like GATK variant-calling and Picard tools, we have a full set of NGS tools at our disposal as Scala classes that are further combined into pipeline functions. Besides meeting the various standard requirements for NGS pipelines such as reentrancy, the BIOPET framework also offers a list of advanced features, such as live debugging, test and meta-analysis frameworks and easy deployment. BIOPET framework can run on various types of HPC infrastructure through its DRMAA support, e.g., SGE, SLURM, PBS.
Peter van't Hof, Szymon M. Kielbasa, Wibowo Arindrarto, Jeroen F. J. Laros, Sander Bollen, Hailiang Mei
CCGrid5
2014 CAFE: an R package for the detection of gross chromosomal abnormalities from gene expression microarray data
abstract
SUMMARY: The current methods available to detect chromosomal abnormalities from DNA microarray expression data are cumbersome and inflexible. CAFE has been developed to alleviate these issues. It is implemented as an R package that analyzes Affymetrix *.CEL files and comes with flexible plotting functions, easing visualization of chromosomal abnormalities. AVAILABILITY AND IMPLEMENTATION: CAFE is available from https://bitbucket.org/cob87icW6z/cafe/ as both source and compiled packages for Linux and Windows. It is released under the GPL version 3 license. CAFE will also be freely available from Bioconductor. CONTACT: [email protected] or [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Sander Bollen, Mathias Leddin, Miguel A. Andrade-Navarro, Nancy Mah
Bioinform.1