clc_assembler
clc_assembler assembles de novo genomic sequences from short-read and long-read next-generation DNA sequencing data to enable genome reconstruction and downstream genomic analyses.
Key Features:
- De Novo Assembly Algorithm: Employs a robust algorithm for de novo assembly of DNA sequencing reads.
- Short- and Long-Read Support: Processes both short-read and long-read sequencing technologies for assembly.
- Integration with Galaxy Project: Provides integration compatibility with the Galaxy Project framework.
- Scalability for Large-Scale Analyses: Supports analysis of large sequencing datasets typical in biomedical and genomic research.
Scientific Applications:
- De Novo Genome Assembly: Reconstruction of genomes from sequencing reads for organisms without reference genomes.
- Non-Model Organism Genomics: Generation of assemblies for non-model organisms to enable gene discovery and comparative studies.
- Metagenomics: Assembly of genomes or genomic fragments from mixed microbial community sequencing data.
- Personalized Medicine: Enabling genome reconstruction to support analyses relevant to personalized medicine.
- Genetic Variation and Gene Discovery: Facilitating exploration of genetic variation and identification of novel genes and genomic elements.
Methodology:
Uses an assembly algorithm optimized for both short-read and long-read next-generation sequencing data to process and assemble DNA sequences efficiently.
Topics
Collections
Details
- Maturity:
- Mature
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 12/19/2016
- Last Updated:
- 11/25/2024
Operations
Data Inputs & Outputs
De-novo assembly
Outputs
Publications
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.
Han H, Cantalupo PG, Rotem A, Cockrell SK, Carbonnaux M, Pipas JM, Weitz DA. Whole‐Genome Sequencing of a Single Viral Species from a Highly Heterogeneous Sample. Angewandte Chemie. 2015;127(47):14191-14194. doi:10.1002/ange.201507047.
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.