Simplifier

Simplifier eliminates redundant sequences from contig collections to reduce redundancy in ab initio genome assemblies and improve assembly metrics for prokaryotic genomes generated from short-read sequencing.


Key Features:

  • Redundancy Elimination: Selectively eliminates redundant sequences from collections of contigs produced by ab initio genome assemblies.
  • Assembly Efficiency: Reduces the number of contigs requiring downstream analysis and integration into complete genome sequences.
  • Performance Metrics: In Corynebacterium pseudotuberculosis strain 258 reduced contigs from 8,004 to 5,272 (34.14%) and increased N50 from 1 kb to 1.5 kb; in Escherichia coli DH10B reduced mate-paired library contigs by 17.47% and fragment library contigs by 23.91%.
  • Target Organisms: Tested on prokaryotic organisms for reducing effort in finalizing genome assemblies from short-read data.

Scientific Applications:

  • Prokaryotic genome assembly: Facilitates reconstruction of complete prokaryotic genomes from fragmented sequences generated by short-read high-throughput sequencing.
  • Post-assembly curation: Supports contig curation workflows and improvement of assembly metrics such as contig counts and N50 for mate-paired and fragment libraries.

Methodology:

Performs selective elimination of redundant sequences from contig collections produced by ab initio genome assemblies.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Ramos RTJ, Carneiro AR, Azevedo V, Schneider MP, Barh D, Silva A. Simplifier: a web tool to eliminate redundant NGS contigs. Bioinformation. 2012;8(20):996-999. doi:10.6026/97320630008996. PMID:23275695. PMCID:PMC3524941.

Documentation

Links