Concepedia

Author

Jonas Behr

Friedrich Miescher LaboratoryORCID

Also Known As

Behr, Jonas, Jonas Behr

26

Publications

1.7K

Citations

13

H-Index

28

Concepts

All Affiliations

Friedrich Miescher LaboratoryMax Planck SocietyETH ZurichSIB Swiss Institute of BioinformaticsMax Planck Institute for Developmental Biology
JB

About

Jonas Behr is an author at Friedrich Miescher Laboratory specializing in genomics, functional genomics, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

234

2

Engineering

2

2

124

3

Health Sciences

1

1

110

4

Biology

1

1

110

5

Biostatistics

1

1

100

Jonas Behr

×

13

Publications

1.7K

Citations

13

H-Index

YearCitations

Multiple reference genomes and transcriptomes for Arabidopsis thaliana

Xiangchao Gan, Oliver Stegle, Jonas Behr,

Nature

2011

676

Nonsense-Mediated Decay of Alternative Precursor mRNA Splicing Variants Is a Major Determinant of the <i>Arabidopsis</i> Steady State Transcriptome

Gabriele Drechsel, André Kahles, Anil K Kesarwani,

The Plant Cell

2013

228

Accurate splice site prediction using support vector machines

Sören Sonnenburg, Gabriele Schweikert, Petra Philips,

BMC Bioinformatics

2007

187

Network-based integration of multi-omics data for prioritizing cancer genes

Christos Dimitrakopoulos, Sravanth K. Hindupur, Luca Häfliger,

Bioinformatics

2018

166

Alternative Splicing Substantially Diversifies the Transcriptome during Early Photomorphogenesis and Correlates with the Energy Availability in Arabidopsis

Lisa Hartmann, Philipp Drewe-Boß, Theresa Wießner,

The Plant Cell

2016

110

mGene: Accurate SVM-based gene finding with an application to nematode genomes

Gabriele Schweikert, Alexander Zien, Georg Zeller,

Genome Research

2009

100

MITIE: Simultaneous RNA-Seq-based transcript identification and quantification in multiple samples

Jonas Behr, André Kahles, Vipin T. Sreedharan,

Bioinformatics

2013

67

MMR: a tool for read multi-mapper resolution

André Kahles, Jonas Behr, Gunnar Rätsch

Bioinformatics

2015

47

Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers

Ariane Leoni Hofmann, Jonas Behr, Jochen Singer,

BMC Bioinformatics

2017

47

Mutational interactions define novel cancer subgroups

Jack Kuipers, Thomas Thurnherr, Giusi Moffa,

Nature Communications

2018

32

Page 1