Andreas Wilm
Molecular Biology · 2005–2021
A researcher in the Science corpus: 8 papers; trusts 15 researchers and is trusted by 7 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 91 citations into it; #4,322 of 17,773 by trust here, #1,188 by citations
- Computational Biology & Bioinformatics — 17 citations into it; #656 of 660 by trust here, #233 by citations
- Artificial Intelligence — 14 citations into it
- Ecology — 8 citations into it; #10,708 of 10,717 by trust here, #1,423 by citations
Whom Andreas Wilm trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Robert C. Edgar
- Sean R. Eddy
- Cédric Notredame
- Kazutaka Katoh
- Temple F. Smith
- Elena Rivas
- Arthur P. Dempster
- Desmond G. Higgins
- Ivo L. Hofacker
- Richard Durbin
Who trusts Andreas Wilm overall
- Kazutaka Katoh
- Fabian Sievers
- Yumeng Yan
- Desmond G. Higgins
- Hiroyuki Toh
- Niko Beerenwinkel
- Audrey A. Burnim
- H. Letsch
- Pei-Zhang Zhou
- Yasuo Tabei
Papers from Andreas Wilm's perspective
Ordered by how strongly the researchers Andreas Wilm trusts endorse each paper. Same corpus, a different order for every researcher.
- T-Coffee: A novel method for fast and accurate multiple sequence alignment.
- Identification of common molecular subsequences.
- MUSCLE: multiple sequence alignment with high accuracy and high throughput.
- MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform.
- Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids
- MUSCLE: a multiple sequence alignment method with reduced time and space complexity
- Progressive sequence alignment as a prerequisitetto correct phylogenetic trees
- Rfam: an RNA family database
- Dynalign: an algorithm for finding the secondary structure common to two RNA sequences. (Journal of Molecular Biology)
- Secondary structure prediction for aligned RNA sequences. (Journal of Molecular Biology)
Their papers
- Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega (2011) — 15,106 citations
- Clustal W and Clustal X version 2.0 (2007) — 27,603 citations
- A benchmark of multiple sequence alignment programs upon structural RNAs (2005) — 302 citations
- LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets (2012) — 1,315 citations
- Fast and sensitive mapping of nanopore sequencing reads with GraphMap (2016) — 346 citations
- The nf-core framework for community-curated bioinformatics pipelines (2020) — 3,308 citations
- Sustainable data analysis with Snakemake (2021) — 1,549 citations
- Large-scale whole-genome sequencing of three diverse Asian populations in Singapore (2018) — 153 citations