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Related Experiment Video

Updated: Feb 8, 2026

Automated Gel Size Selection to Improve the Quality of Next-generation Sequencing Libraries Prepared from Environmental Water Samples
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Crumble: reference free lossy compression of sequence quality values.

James K Bonfield1, Shane A McCarthy1,2, Richard Durbin1,2

  • 1DNA Pipelines, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.

Bioinformatics (Oxford, England)
|July 12, 2018
PubMed
Summary
This summary is machine-generated.

A new tool, Crumble, significantly reduces the size of Next-Generation Sequencing (NGS) CRAM files by compressing quality scores. This method achieves substantial file size reduction without compromising variant calling accuracy.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Data Compression

Background:

  • Next-Generation Sequencing (NGS) generates large CRAM files, with a significant portion of the storage occupied by per-base quality values.
  • Many of these quality values are redundant for variant calling, presenting an opportunity for data compression and storage optimization.

Purpose of the Study:

  • To develop and evaluate a method for reducing the storage space of CRAM files by selectively compressing quality score data.
  • To assess the impact of this compression on variant calling accuracy.

Main Methods:

  • Implementation of an open-source tool named Crumble for compressing quality data within CRAM files.
  • Testing the tool on the Syndip dataset to measure the reduction in quality storage and overall file size.
  • Evaluating variant calling accuracy after data compression.

Main Results:

  • Achieved a 17-fold reduction in the quality storage portion of CRAM files on the Syndip test set.
  • Observed overall CRAM file size reductions ranging from 2.2 to 7.4 fold, dependent on the file's non-quality content.
  • Maintained variant calling accuracy despite significant data compression.

Conclusions:

  • Crumble offers an effective strategy for reducing CRAM file sizes by optimizing the storage of quality values.
  • The tool provides substantial space savings without sacrificing the integrity of variant calling results.
  • This approach has the potential to alleviate storage burdens in large-scale genomics projects.