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Andreas Wilm

Researcher at Genome Institute of Singapore

Publications -  48
Citations -  43460

Andreas Wilm is an academic researcher from Genome Institute of Singapore. The author has contributed to research in topics: Population & Multiple sequence alignment. The author has an hindex of 28, co-authored 46 publications receiving 37117 citations. Previous affiliations of Andreas Wilm include University College Dublin & Swiss Institute of Bioinformatics.

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Clustal W and Clustal X version 2.0

TL;DR: The Clustal W and ClUSTal X multiple sequence alignment programs have been completely rewritten in C++ to facilitate the further development of the alignment algorithms in the future and has allowed proper porting of the programs to the latest versions of Linux, Macintosh and Windows operating systems.
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LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets

TL;DR: It is shown that LoFreq has near-perfect specificity, with significantly improved sensitivity compared with existing methods and can efficiently analyze deep Illumina sequencing datasets without resorting to approximations or heuristics.
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The nf-core framework for community-curated bioinformatics pipelines.

TL;DR: The nf-core framework is introduced as a means for the development of collaborative, peerreviewed, best-practice analysis pipelines that can be used across all institutions and research facilities and introduces a higher degree of portability as compared to custom in-house scripts.