Tobias Rausch
Researcher Next ID · RN-030085
Researcher · Biochemistry, Genetics and Molecular Biology
European Molecular Biology Laboratory
Heidelberg, Germany
- Works count
- 253
- Citation count
- 85,737
- H-index
- 62
- i10-index
- 107
Research interests
Publications
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
Cell · 2022 · https://doi.org/10.1016/j.cell.2022.08.004
Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes
Nature Genetics · 2022 · 10.1038/s41588-022-01043-w
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
Science · 2021 · https://doi.org/10.1126/science.abf7117
Human-specific tandem repeat expansion and differential gene expression during primate evolution
Proceedings of the National Academy of Sciences · 2019 · https://doi.org/10.1073/pnas.1912175116
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Nature Communications · 2019 · https://doi.org/10.1038/s41467-018-08148-z
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
The Lancet Oncology · 2018 · https://doi.org/10.1016/s1470-2045(18)30242-0
An integrated map of structural variation in 2,504 human genomes
Nature · 2015 · https://doi.org/10.1038/nature15394
Assembly and diploid architecture of an individual human genome via single-molecule technologies
Nature Methods · 2015 · https://doi.org/10.1038/nmeth.3454
Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition
Cancer Cell · 2014 · https://doi.org/10.1016/j.ccr.2014.02.004
Integrative Genomic Analyses Reveal an Androgen-Driven Somatic Alteration Landscape in Early-Onset Prostate Cancer
Cancer Cell · 2013 · https://doi.org/10.1016/j.ccr.2013.01.002
The Genomic and Transcriptomic Landscape of a HeLa Cell Line
G3 Genes Genomes Genetics · 2013 · https://doi.org/10.1534/g3.113.005777
DELLY: structural variant discovery by integrated paired-end and split-read analysis
Bioinformatics · 2012 · https://doi.org/10.1093/bioinformatics/bts378
Dissecting the genomic complexity underlying medulloblastoma
Nature · 2012 · 10.1038/nature11284
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Nature · 2012 · https://doi.org/10.1038/nature10833
Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations
Cell · 2012 · 10.1016/j.cell.2011.12.013
Mapping copy number variation by population-scale genome sequencing
Nature · 2011 · https://doi.org/10.1038/nature09708
SeqAn An efficient, generic C++ library for sequence analysis
BMC Bioinformatics · 2008 · 10.1186/1471-2105-9-11
Current projects
No projects listed.