clc_sequence_info

clc_sequence_info extracts and summarizes metadata and assembly-related metrics from sequence files to support transcriptome assembly analysis of high-throughput sequencing data such as Roche 454 pyrosequencing producing short reads (250–450 base pairs).


Key Features:

  • Data Handling and Assembly: Supports processing of sequence files produced by Roche 454 pyrosequencing and the assembly of short reads into longer contigs for transcript reconstruction.
  • Assembler Comparison and Optimization: Incorporates methodologies from systematic comparisons of assemblers including CAP3, MIRA, Newbler, SeqMan, and CLC and leverages combining outputs from multiple assemblers to improve assembly credibility.
  • Statistical and Computational Analysis: Applies statistical methods to handle large next-generation sequencing datasets and derive metrics relevant to assembly evaluation.
  • Tracking and Documentation: Records and documents computational steps and assembly merges to support reproducibility of analyses.

Scientific Applications:

  • Transcriptome Assembly: Supports assembly of transcriptomes from non-model organisms using short-read Roche 454 data for downstream gene expression and functional annotation analyses.
  • Assembly Merging and Integration: Facilitates merging of assemblies from different programs to produce more consistent and reliable consensus transcript sets.
  • Reproducible Computational Workflows: Enables reproducible reporting of computational steps and assembly decisions for data integration and verification.

Methodology:

Processes Roche 454 sequence files; assembles short reads into contigs; performs systematic comparisons of assemblers (CAP3, MIRA, Newbler, SeqMan, CLC); merges outputs from multiple assemblers; applies statistical analyses to large datasets; records computational steps.

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

Format detection

Publications

Kumar S, Blaxter ML. Comparing de novo assemblers for 454 transcriptome data. BMC Genomics. 2010;11(1). doi:10.1186/1471-2164-11-571. PMID:20950480. PMCID:PMC3091720.

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.

Links