Tobias Marschall
Molecular Biology · 2015–2022
A researcher in the Science corpus: 12 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 387 citations into it
- Genetics — 177 citations into it
- Artificial Intelligence — 33 citations into it
Whom Tobias Marschall trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Tobias Marschall's perspective
Ordered by how strongly the researchers Tobias Marschall trusts endorse each paper. Same corpus, a different order for every researcher.
- MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
- Haplotype phasing: Existing methods and new developments (Nature reviews genetics)
- Diversity of Human Copy Number Variation and Multicopy Genes (Science)
- Limitations of next-generation genome sequence assembly (Nature Methods)
- Mapping copy number variation by population scale genome sequencing (Nature)
- Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. (Genetics)
- RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. (American Journal of Human Genetics)
- A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies (PLoS Genetics)
Their papers
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) — 1,512 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- WhatsHap: Weighted Haplotype Assembly for Future-Generation Sequencing Reads (2015) — 410 citations
- The Human Pangenome Project: a global resource to map genomic diversity (2022) — 392 citations
- A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
- Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes (2020) — 428 citations
- The complete sequence of a human genome (2021) — 2,469 citations
- Eleven grand challenges in single-cell data science (2020) — 1,198 citations
- Mapping and phasing of structural variation in patient genomes using nanopore sequencing (2017) — 370 citations
- A draft human pangenome reference (2022) — 882 citations
- Haplotype-resolved diverse human genomes and integrated analysis of structural variation (2021) — 639 citations
- WhatsHap: fast and accurate read-based phasing (2016) — 406 citations