clc_mapping_info

clc_mapping_info analyzes read mapping data from Roche 454 pyrosequencing (250–450 base pairs) to report mapping details that support evaluation and interpretation of transcriptome assemblies.


Key Features:

  • Read Mapping Analysis: Provides detailed information about how individual sequencing reads align to reference sequences or assembled contigs.
  • Integration with Assembly Tools: Complements transcriptome assemblers such as CAP3, MIRA, Newbler, SeqMan, and CLC by reporting mapping quality and coverage metrics for assembled contigs.
  • Support for Multiple Assemblers: Accepts and interprets outputs from different assemblers to enable evaluation and comparison of assembly strategies.
  • Enhanced Data Interpretation: Supplies mapping-derived metrics to identify issues such as redundant contigs and variable read coverage across assemblies.

Scientific Applications:

  • Transcriptome Assembly Optimization: Assesses assembly quality for Roche 454 transcriptome datasets (250–450 bp) to inform selection of assembly parameters and tools.
  • Data Integration and Merging: Supports merging assemblies from different programs to improve alignment consistency and contig size uniformity.
  • Comparative Analysis: Enables systematic comparison of assembler performance using metrics such as contig length, novelty, and redundancy derived from mappings.
  • High-throughput Sequencing Data Management: Facilitates management and interpretation of read mapping and assembly outputs from high-throughput sequencing experiments.

Methodology:

Analyzes read mappings to evaluate contig length and quality, alignments to reference sequences or assembled contigs, and coverage distribution across assembled transcripts.

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

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.

Documentation

Links