Tobias Marschall integrates Gene and Evolutionary biology in his research. He performs integrative Evolutionary biology and Gene research in his work. As part of his studies on Genetics, he often connects relevant areas like Sequence (biology). His research links Genetics with Sequence (biology). His work often combines Genome and Germline studies. He incorporates Germline and Genome in his studies. He connects Computational biology with Algorithm in his study. He combines Algorithm and Computational biology in his research. Tobias Marschall conducts interdisciplinary study in the fields of Human genome and Human genetics through his research.
Indel and 1000 Genomes Project are the focus of his Single-nucleotide polymorphism studies. Indel connects with themes related to Single-nucleotide polymorphism in his study. Gene and Evolutionary biology are two areas of study in which he engages in interdisciplinary work. He conducted interdisciplinary study in his works that combined Evolutionary biology and Gene. Many of his studies involve connections with topics such as Sequence (biology) and Genetics. His research on Sequence (biology) often connects related areas such as Genetics. Tobias Marschall combines Genome and Genotyping in his research. In his study, he carries out multidisciplinary Genotyping and Genotype research. His Genotype study often links to related topics such as 1000 Genomes Project.
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Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome.
Aaron M. Wenger;Paul Peluso;William J. Rowell;Pi-Chuan Chang.
Nature Biotechnology (2019)
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Mark J.P. Chaisson;Mark J.P. Chaisson;Ashley D. Sanders;Xuefang Zhao;Xuefang Zhao;Ankit Malhotra.
Nature Communications (2019)
Eleven grand challenges in single-cell data science
David Lähnemann;David Lähnemann;Johannes Köster;Johannes Köster;Ewa Szczurek;Davis J. McCarthy;Davis J. McCarthy.
Genome Biology (2020)
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Mircea Cretu Stancu;Markus J. van Roosmalen;Ivo Renkens;Marleen M. Nieboer.
Nature Communications (2017)
WhatsHap: Weighted Haplotype Assembly for Future-Generation Sequencing Reads
Murray Patterson;Tobias Marschall;Nadia Pisanti;Leo van Iersel.
Journal of Computational Biology (2015)
Computational pan-genomics: status, promises and challenges.
Tobias Marschall;Manja Marz;Manja Marz;Thomas Abeel;Louis Dijkstra.
Briefings in Bioinformatics (2018)
Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes.
Kishwar Shafin;Trevor Pesout;Ryan Lorig-Roach;Marina Haukness.
Nature Biotechnology (2020)
Haplotype-resolved diverse human genomes and integrated analysis of structural variation.
Peter Ebert;Peter A. Audano;Qihui Zhu;Bernardo Rodriguez-Martin.
A robust benchmark for detection of germline large deletions and insertions.
Justin M. Zook;Nancy F. Hansen;Nathan D. Olson;Lesley Chapman.
Nature Biotechnology (2020)
WhatsHap: fast and accurate read-based phasing
M. Martin;Patterson;S. Garg (Shilpa);S. Fischer.
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