Tobias Rausch
Nature · 2008–2021
A researcher in the Science corpus: 12 papers; trusts 1 researcher and is trusted by 3 researchers here, as inferred from the citation graph.
Whom Tobias Rausch trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Tobias Rausch overall
Papers from Tobias Rausch's perspective
Ordered by how strongly the researchers Tobias Rausch trusts endorse each paper. Same corpus, a different order for every researcher.
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Exome sequencing as a tool for Mendelian disease gene discovery
- The Human Gene Mutation Database: 2008 update
- Mapping copy number variation by population scale genome sequencing (Nature)
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- The origin and evolution of mutations in Acute Myeloid Leukemia (Cell)
- Basic local alignment search tool.
- International network of cancer genome projects (Nature)
- A whole-genome assembly of Drosophila. (Science)
Their papers
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- SeqAn An efficient, generic C++ library for sequence analysis (2008) — 381 citations
- Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma (2012) — 2,412 citations
- Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations (2012) — 858 citations
- Bioconda: sustainable and comprehensive software distribution for the life sciences (2018) — 1,435 citations
- DELLY: structural variant discovery by integrated paired-end and split-read analysis (2012) — 2,205 citations
- Dissecting the genomic complexity underlying medulloblastoma (2012) — 847 citations
- Haplotype-resolved diverse human genomes and integrated analysis of structural variation (2021) — 639 citations
- An integrated map of structural variation in 2,504 human genomes (2015) — 2,247 citations
- Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition (2014) — 693 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Mapping copy number variation by population scale genome sequencing (2011) — 1,130 citations