Fritz J. Sedlazeck
Molecular Biology · 2013–2024
A researcher in the Science corpus: 15 papers; trusts 29 researchers and is trusted by 5 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 362 citations into it; #7,476 of 17,773 by trust here, #2,878 by citations
- Genetics — 165 citations into it; #3,977 of 6,854 by trust here, #1,130 by citations
- Artificial Intelligence — 49 citations into it
- Ecology — 30 citations into it
- Computational Biology & Bioinformatics — 18 citations into it
Whom Fritz J. Sedlazeck trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Eugene W. Myers
- Genome analysis
- Mark J. P. Chaisson
- Ben Langmead
- Gerton A. Lunter
- Steven L. Salzberg
- Sara Goodwin
- Nicholas J. Loman
- Sharon R. Browning
Who trusts Fritz J. Sedlazeck overall
- Heng Li
- Davide Heller
- M. Mahmoud
- Sergey Koren
- Aaron M. Wenger
- Yunhao Wang
- Martin Vingron
- Arang Rhie
- Michael Alonge
- C. Peñaloza
Papers from Fritz J. Sedlazeck's perspective
Ordered by how strongly the researchers Fritz J. Sedlazeck trusts endorse each paper. Same corpus, a different order for every researcher.
- Assembling large genomes with single-molecule sequencing and locality-sensitive hashing (Nature Biotechnology)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
- The human genome browser at UCSC.
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- IDBA - A Practical Iterative de Bruijn Graph De Novo Assembler (Annual International Conference on Research in Computational Molecular Biology)
- A whole-genome assembly of Drosophila. (Science)
- Real-Time DNA Sequencing from Single Polymerase Molecules (Science)
- RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. (American Journal of Human Genetics)
Their papers
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) — 1,512 citations
- Phased Diploid Genome Assembly with Single Molecule Real-Time Sequencing (2016) — 1,743 citations
- Transient structural variations have strong effects on quantitative traits and reproductive isolation in fission yeast (2017) — 674 citations
- Accurate detection of complex structural variations using single molecule sequencing (2017) — 1,457 citations
- Piercing the dark matter: bioinformatics of long-range sequencing and mapping (2018) — 461 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
- NextGenMap: fast and accurate read mapping in highly polymorphic genomes (2013) — 427 citations
- Structural variant calling: the long and the short of it (2019) — 588 citations
- Detection of mosaic and population-level structural variants with Sniffles2 (2024) — 386 citations
- Major impacts of widespread structural variation on gene expression and crop improvement in tomato (2020) — 629 citations
- RaGOO: fast and accurate reference-guided scaffolding of draft genomes (2019) — 586 citations
- GenomeScope: Fast reference-free genome profiling from short reads (2016) — 1,665 citations
- Updating benchtop sequencing performance comparison (2013) — 494 citations