noisy

noisy identifies and removes phylogenetically uninformative and homoplastic sites from nucleic acid multiple sequence alignments to mitigate alignment errors and improve phylogenetic reconstruction.


Key Features:

  • Identification of uninformative sites: Assesses the distribution of character states along a cyclic ordering of taxa within a multiple sequence alignment to detect homoplastic and randomized sites.
  • Site filtering to improve trees: Removes identified uninformative sites to increase stability and indices of tree quality in downstream phylogenetic reconstruction.
  • Applicability conditions: Particularly effective for datasets with large evolutionary distances, variable substitution rates, low average bootstrap support, and when at least 12 to 15 taxa are present.

Scientific Applications:

  • Phylogenetic reconstruction refinement: Reduces misleading signal from homoplasies and alignment errors in nucleic acid-based phylogenies.
  • Analyses of deep divergences and heterogeneous datasets: Enhances accuracy and stability of trees for datasets with large evolutionary distances and heterogeneous substitution rates.

Methodology:

Assesses character state distributions within a cyclic ordering of taxa in a multiple sequence alignment and removes sites identified as homoplastic or strongly randomized.

Topics

Collections

Details

Maturity:
Mature
Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Programming Languages:
C++
Added:
12/19/2016
Last Updated:
11/25/2024

Operations

Publications

Dress AW, Flamm C, Fritzsch G, Grünewald S, Kruspe M, Prohaska SJ, Stadler PF. Noisy: Identification of problematic columns in multiple sequence alignments. Algorithms for Molecular Biology. 2008;3(1). doi:10.1186/1748-7188-3-7. PMID:18577231. PMCID:PMC2464588.

Afgan E, Baker D, van den Beek M, Blankenberg D, Bouvier D, Čech M, Chilton J, Clements D, Coraor N, Eberhard C, Grüning B, Guerler A, Hillman-Jackson J, Von Kuster G, Rasche E, Soranzo N, Turaga N, Taylor J, Nekrutenko A, Goecks J. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update. Nucleic Acids Research. 2016;44(W1):W3-W10. doi:10.1093/nar/gkw343. PMID:27137889. PMCID:PMC4987906.

Mareuil F, Doppelt-Azeroual O, Ménager H. A public Galaxy platform at Pasteur used as an execution engine for web services. Unknown Journal. 2017. doi:10.7490/f1000research.1114334.1.

Documentation

Links