Sebastian Schönherr

发表

Delivering bioinformatics MapReduce applications in the cloud

Tomislav Lipic, Enis Afgan, Davor Davidovic, 2014, 2014 37th International Convention on Information and Communication Technology, Electronics and Microelectronics (MIPRO).

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Giovanni Malerba, Jin Li, Rohit Varma, 2017, Nature Genetics.

Cloudflow - enabling faster biomedical pipelines with MapReduce and Spark

Günther Specht, Enis Afgan, Davor Davidovic, 2016, Scalable Comput. Pract. Exp..

LASER server: ancestry tracing with genotypes or sequence reads

Michael Boehnke, Lukas Forer, Sebastian Schönherr, 2017, Bioinform..

HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing

Hans-Jürgen Bandelt, Günther Specht, Lukas Forer, 2016, Nucleic Acids Res..

mtDNA-Server: next-generation sequencing data analysis of human mitochondrial DNA in the cloud

Günther Specht, Lukas Forer, Sebastian Schönherr, 2016, Nucleic Acids Res..

Synchronous metadata management of large storage systems

Günther Specht, Sebastian Schönherr, Günter Hackl, 2010, IDEAS '10.

Cloudflow - A framework for MapReduce pipeline development in Biomedical Research

Günther Specht, Enis Afgan, Davor Davidovic, 2015, 2015 38th International Convention on Information and Communication Technology, Electronics and Microelectronics (MIPRO).

CONAN: copy number variation analysis software for genome-wide association studies

Günther Specht, Lukas Forer, Sebastian Schönherr, 2010, BMC Bioinformatics.

Cloudgene: A graphical execution platform for MapReduce programs on private and public clouds

Günther Specht, Lukas Forer, Sebastian Schönherr, 2012, BMC Bioinformatics.

eCOMPAGT integrates mtDNA: import, validation and export of mitochondrial DNA profiles for population genetics, tumour dynamics and genotype-phenotype association studies

Günther Specht, Sebastian Schönherr, Hansi Weißensteiner, 2010, BMC Bioinformatics.

A feedback guided interface for elastic computing

Lukas Forer, Sebastian Schönherr, Hansi Weißensteiner, 2011, Grundlagen von Datenbanken.

eCOMPAGT – efficient Combination and Management of Phenotypes and Genotypes for Genetic Epidemiology

Günther Specht, Sebastian Schönherr, Hansi Weißensteiner, 2009, BMC Bioinformatics.

Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma

Lukas Forer, Sebastian Schönherr, Florian Kronenberg, 2015, PloS one.

Experiences with workflows for automating data-intensive bioinformatics

Ola Spjuth, Eija Korpelainen, Samuel Lampa, 2015, Biology Direct.

HaploGrep: a fast and reliable algorithm for automatic classification of mitochondrial DNA haplogroups

Günther Specht, Sebastian Schönherr, Florian Kronenberg, 2011, Human mutation.