A novel and well-defined benchmarking method for second generation read mapping
2011

A New Benchmark Method for Read Mapping

publication Evidence: high

Author Information

Author(s): Holtgrewe Manuel, Emde Anne-Katrin, Weese David, Reinert Knut

Primary Institution: Free University of Berlin

Hypothesis

The study proposes a novel benchmarking method for evaluating read mappers in second generation sequencing.

Conclusion

The benchmark program effectively compares popular read mappers and provides tools for evaluating their performance.

Supporting Evidence

  • The benchmark method allows for the generation of gold standards for both simulated and real-world reads.
  • It helps to objectively compare different read mapping programs.
  • The study highlights the importance of careful benchmarking in advancing read mapping research.

Takeaway

This study created a new way to test how well different programs can match DNA sequences, helping scientists choose the best one for their needs.

Methodology

The study defines the read mapping problem and introduces a benchmark method called Rabema to evaluate read mappers.

Limitations

The method is currently limited to base-space reads and does not incorporate mate pair information or quality values.

Digital Object Identifier (DOI)

10.1186/1471-2105-12-210

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