Contact

email

stephan.pabinger@gmail.com

mail address

AIT Austrian Institute of Technology GmbH
Giefinggasse 4
1210 Vienna
Austria

about

I am a scientist in the Molecular Diagnostics Unit at the Austrian Institute of Technology.

cv

PDF

web

View Stephan Pabinger's profile on LinkedIn   View Stephan Pabinger's profile on GitHub   View Stephan Pabinger's profile on GitHub

View Stephan Pabinger's ORCID profile  
  

Talks

Research Interests

(*) Analysis of high-throughput biological data - especially next-generation sequencing data

(*) Development of bioinformatics methods and tools (NGS, Assembly, QPCR, ...)

(*) Epigenetics

(*) Integration of heterogeneous high-throughput data

(*) Multivariate data analysis

Publications

Maghuly F, Pabinger S, Krainer J, Laimer M.
The Pattern and Distribution of Induced Mutations in J. curcas Using Reduced Representation Sequencing.
Front Plant Sci 2018. pubmed

Hendling M, Pabinger S, Peters K, Wolff N, Conzemius R, Barišic I.
Oli2go: an automated multiplex oligonucleotide design tool.
Nucleic Acids Res. 2018. pubmed

Gencay M, Seffner A, Pabinger S, Gautier J, Gohl P, Weizenegger M, Neofytos D, Batrla R, Woeste A, Kim HS, Westergaard G, Reinsch C, Brill E, Thuy PTT, Hoang BH, Sonderup M, Spearman CW, Brancaccio G, Fasano M, Gaeta GB, Santantonio T, Kaminski WE.
Detection of in vivo hepatitis B virus surface antigen mutations-A comparison of four routine screening assays.
J. Viral Hepat. 2018. pubmed

Kim HS, Chen X, Xu M, Yan C, Liu Y, Deng H, Hoang BH, Thuy PTT, Wang T, Yan Y, Zeng Z, Gencay M, Westergaard G, Pabinger S, Kriegner A, Nauck M, Seffner A, Gohl P, Hübner K, Kaminski WE.
Frequency of hepatitis B surface antigen variants (HBsAg) in hepatitis B virus genotype B and C infected East- and Southeast Asian patients: Detection by the Elecsys® HBsAg II assay.
J. Clin. Virol. 2018. pubmed

Gencay M, Vermeulen M, Neofytos D, Westergaard G, Pabinger S, Kriegner A, Seffner A, Gohl P, Huebner K, Nauck M, Kaminski WE.
Substantial variation in the hepatitis B surface antigen (HBsAg) in hepatitis B virus (HBV)-positive patients from South Africa: Reliable detection of HBV by the Elecsys HBsAg II assay.
J. Clin. Virol. 2018. pubmed

Gencay M, Hübner K, Gohl P, Seffner A, Weizenegger M, Neofytos D, Batrla R, Woeste A, Kim HS, Westergaard G, Reinsch C, Brill E, Thu Thuy PT, Hoang BH, Sonderup M, Spearman CW, Pabinger S, Gautier J, Brancaccio G, Fasano M, Santantonio T, Gaeta GB, Nauck M, Kaminski WE.
Ultra-deep sequencing reveals high prevalence and broad structural diversity of hepatitis B surface antigen mutations in a global population.
PLoS ONE 2017. pubmed

Pandey RV, Pabinger S, Kriegner A, Weinhäusel A.
DaMold: A data-mining platform for variant annotation and visualization in molecular diagnostics research.
Hum. Mutat. 2017. pubmed

Pandey RV, Pulverer W, Kallmeyer R, Beikircher G, Pabinger S, Kriegner A, Weinhäusel A.
MSP-HTPrimer: a high-throughput primer design tool to improve assay design for DNA methylation analysis in epigenetics.
Clin Epigenetics 2016. pubmed

Pabinger S, Ernst K, Pulverer W, Kallmeyer R, Valdes AM, Metrustry S, Katic D, Nuzzo A, Kriegner A, Vierlinger K, Weinhaeusel A.
Analysis and Visualization Tool for Targeted Amplicon Bisulfite Sequencing on Ion Torrent Sequencers.
PLoS ONE 2016. pubmed

Pandey RV, Pulverer W, Kallmeyer R, Beikircher G, Pabinger S, Kriegner A, Weinhäusel A.
MSRE-HTPrimer: a high-throughput and genome-wide primer design pipeline optimized for epigenetic research.
Clin Epigenetics 2016. pubmed

Pandey RV, Pabinger S, Kriegner A, Weinhäusel A.
MutAid: Sanger and NGS Based Integrated Pipeline for Mutation Identification, Validation and Annotation in Human Molecular Genetics.
PLoS ONE 2016. pubmed

Pandey RV, Pabinger S, Kriegner A, Weinhäusel A.
ClinQC: a tool for quality control and cleaning of Sanger and NGS data in clinical research.
BMC Bioinformatics 2016. pubmed

Friedrich V, Pabinger S, Chen T, Messner P, Dewhirst FE, Schäffer C.
Draft Genome Sequence of Tannerella forsythia Type Strain ATCC 43037.
Genome Announc 2015. pubmed

Friedrich V, Gruber C, Nimeth I, Pabinger S, Sekot G, Posch G, Altmann F, Messner P, Andrukhov O, Schäffer C.
Outer membrane vesicles of Tannerella forsythia: biogenesis, composition, and virulence.
Mol Oral Microbiol 2015. pubmed

Maghuly F, Jankowicz-Cieslak J, Pabinger S, Till BJ, Laimer M.
Geographic origin is not supported by the genetic variability found in a large living collection of Jatropha curcas with accessions from three continents.
Biotechnol J 2015. pubmed

Pabinger S, Rödiger S, Kriegner A, Vierlinger K, Weinhäusel A.
A survey of tools for the analysis of quantitative PCR (qPCR) data.
Biomol Detect Quantif 2014. pubmed

Dander A, Baldauf M, Sperk M, Pabinger S, Hiltpolt B, Trajanoski Z.
Personalized Oncology Suite: integrating next-generation sequencing data and whole-slide bioimages.
BMC Bioinformatics 2014. pubmed

Schweiger D, Trajanoski Z, Pabinger S.
SPARQLGraph: a web-based platform for graphically querying biological Semantic Web databases.
BMC Bioinformatics 2014. pubmed

Pabinger S, Snajder R, Hardiman T, Willi M, Dander A, Trajanoski Z.
MEMOSys 2.0: an update of the bioinformatics database for genome-scale models and genomic data.
Database (Oxford) 2014. pubmed

Dander A, Pabinger S, Sperk M, Fischer M, Stocker G, Trajanoski Z.
SeqBench: integrated solution for the management and analysis of exome sequencing data.
BMC Res Notes 2014. pubmed

Dander A, Mueller LA, Gallasch R, Pabinger S, Emmert-Streib F, Graber A, Dehmer M.
[COMMODE] a large-scale database of molecular descriptors using compounds from PubChem.
Source Code Biol Med 2013. pubmed

Magoc T, Pabinger S, Canzar S, Liu X, Su Q, Puiu D, Tallon LJ, Salzberg SL.
GAGE-B: an evaluation of genome assemblers for bacterial organisms.
Bioinformatics 2013. pubmed

Pabinger S, Dander A, Fischer M, Snajder R, Sperk M, Efremova M, Krabichler B, Speicher MR, Zschocke J, Trajanoski Z.
A survey of tools for variant analysis of next-generation genome sequencing data.
Brief. Bioinformatics 2014. pubmed

Pabinger S, Trajanoski Z.
Genome-scale model management and comparison.
Methods Mol. Biol. 2013. pubmed

Fischer M, Snajder R, Pabinger S, Dander A, Schossig A, Zschocke J, Trajanoski Z, Stocker G.
SIMPLEX: cloud-enabled pipeline for the comprehensive analysis of exome sequencing data.
PLoS ONE 2012. pubmed

Schossig A, Wolf NI, Fischer C, Fischer M, Stocker G, Pabinger S, Dander A, Steiner B, Tönz O, Kotzot D, Haberlandt E, Amberger A, Burwinkel B, Wimmer K, Fauth C, Grond-Ginsbach C, Koch MJ, Deichmann A, von Kalle C, Bartram CR, Kohlschütter A, Trajanoski Z, Zschocke J.
Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome.
Am. J. Hum. Genet. 2012. pubmed

Pabinger S, Rader R, Agren R, Nielsen J, Trajanoski Z.
MEMOSys: Bioinformatics platform for genome-scale metabolic models.
BMC Syst Biol 2011. pubmed

Pabinger S, Thallinger GG, Snajder R, Eichhorn H, Rader R, Trajanoski Z.
QPCR: Application for real-time PCR data management and analysis.
BMC Bioinformatics 2009. pubmed

Software

oli2go

A tool for multiplex oligonucleotide design. More information here.

TABSAT

analysis of targeted bisulfite sequencing data generated on an Ion Torrent PGM / Illumina MiSeq.

QPCR

web application to store and analyze data from qPCR experiments. More information here.

MEMOSys

bioinformatics platform for the management and development of metabolic models.

SIMPLEX

cloud-enabled pipeline for the comprehensive analysis of exome sequencing data.

SPARQLGraph

visual query builder for biological RDF databases. Winner of the EBI RDFApp competition.

DaMold

Data-mining platform for variant annotation and visualization.

PRINSEQ Parallel

parallelized, multithreading version of PRINSEQ.