Henrik Bengtsson

发表

A Probe-Level Data File Format Used by 'aroma.affymetrix'[deprecated]

Henrik Bengtsson, 2015 .

Henrik Bengtsson, H. Bengtsson, 2004 .

Methodological study of affine transformations of gene expression data with proposed robust non-parametric multi-dimensional normalization method

Henrik Bengtsson, Ola Hössjer, O. Hössjer, 2006, BMC Bioinformatics.

Analysis of Large Affymetrix Microarray Data Sets

Henrik Bengtsson, 2016 .

Methods and arrangements for the distribution of applications

Henrik Bengtsson, Troed Sangberg, Ola Montan, 2007 .

Querying Genomic Databases: Refining the Connectivity Map

Robert Gentleman, Hao Xiong, Henrik Bengtsson, 2012, Statistical applications in genetics and molecular biology.

Reconstruction of 3D genome architecture via a two-stage algorithm

Mark R. Segal, Henrik Bengtsson, M. Segal, 2015, BMC Bioinformatics.

A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6

Terence P. Speed, Henrik Bengtsson, Pratyaksha Wirapati, 2009, Bioinform..

Microarray image analysis: background estimation using quantile and morphological filters

Henrik Bengtsson, Anders Bengtsson, 2005, BMC Bioinformatics.

Identification and normalization of plate effects in cDNA Microarray data

Henrik Bengtsson, 2002 .

Improved accuracy assessment for 3D genome reconstructions

Mark R. Segal, Henrik Bengtsson, M. Segal, 2018, BMC Bioinformatics.

The R.oo package - Object-oriented programming with references using standard R code

Henrik Bengtsson, H. Bengtsson, 2003 .

Calibration and assessment of channel-specific biases in microarray data with extended dynamical range

Johan Vallon-Christersson, Henrik Bengtsson, Göran Jönsson, 2004, BMC Bioinformatics.

A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods

Terence P. Speed, Paul T. Spellman, Henrik Bengtsson, 2009, Bioinform..

aroma - An R object-oriented microarray analysis environment

Henrik Bengtsson, H. Bengtsson, 2004 .

TumorBoost: Normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays

Terence P. Speed, Pierre Neuvial, Henrik Bengtsson, 2010, BMC Bioinformatics.

Parent-specific copy number in paired tumor-normal studies using circular binary segmentation

Paul T. Spellman, Richard A. Olshen, Adam B. Olshen, 2011, Bioinform..

Protocol for wireless real-time systems

Per-Arne Wiberg, Elisabeth Uhlemann, Henrik Bengtsson, 1999, Proceedings of 11th Euromicro Conference on Real-Time Systems. Euromicro RTS'99.

Estimation and assessment of raw copy numbers at the single locus level

Terence P. Speed, Rafael A. Irizarry, Henrik Bengtsson, 2008, Bioinform..

A Measurement Framework for Team Level Assessment of Innovation Capability in Early Requirements Engineering

Martin Höst, Björn Regnell, Fredrik Nilsson, 2009, PROFES.

Discovering hotspots in functional genomic data superposed on 3D chromatin configuration reconstructions

Daniel Capurso, Henrik Bengtsson, Mark R Segal, 2016, Nucleic acids research.

Normal nigrostriatal innervation but dopamine dysfunction in mice carrying hypomorphic tyrosine hydroxylase alleles

Eva Lindqvist, Henrik Bengtsson, Lars Olson, 2003, Journal of neuroscience research.

illuminaio: An open source IDAT parsing tool for Illumina microarrays

Matthew E. Ritchie, Keith A. Baggerly, Kasper D. Hansen, 2013, F1000Research.

Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data.

Rafael A Irizarry, Terence P Speed, Henrik Bengtsson, 2006, Biostatistics.

Statistical Analysis of Single Nucleotide Polymorphism Microarrays in Cancer Studies

Terence P. Speed, Pierre Neuvial, Henrik Bengtsson, 2011 .

Validating the Use of Google Trends to Enhance Pertussis Surveillance in California

W. John Boscardin, Henrik Bengtsson, Simon Pollett, 2015, PLoS currents.

DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly

Pieter Wesseling, Mark A van de Wiel, Bauke Ylstra, 2014, Genome research.