GVC

GVC compresses gene sequence variations generated by high-throughput sequencing technologies while preserving random access to enable efficient storage and retrieval of genotype data.


Key Features:

  • Binarization: Applies binarization to represent variation data prior to further processing.
  • Joint row- and column-wise sorting: Performs joint row- and column-wise sorting of variation blocks to improve local structure for compression.
  • JBIG entropy coding: Uses the image compression standard JBIG for entropy coding of the processed variation blocks.
  • Random-access compression: Maintains random access to compressed variation blocks to allow retrieval of specific segments without full decompression.
  • Demonstrated compression performance: Compresses 1000 Genomes Project (phase 3) genotype information from 758 GiB to 890 MiB, outperforming current state-of-the-art random-access capable methods by 21%.

Scientific Applications:

  • Precision medicine: Reduces storage and enables selective retrieval of variant data used in genotype-driven clinical analyses.
  • Oncology: Supports storage and access of large variant datasets relevant to cancer genomics studies.
  • Food quality control: Enables compressed storage and targeted access of genetic variation data used in food quality and safety applications.
  • Remote data retrieval and integration: Facilitates remote access to specific compressed genomic segments for integration with downstream applications.
  • Large-scale genomic data management: Lowers storage footprint and improves manageability of population-scale genotype datasets.

Methodology:

Uses binarization, joint row- and column-wise sorting of variation blocks, and JBIG for entropy coding.

Topics

Details

Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python
Added:
8/30/2023
Last Updated:
8/30/2023

Operations

Publications

Adhisantoso YG, Voges J, Rohlfing C, Tunev V, Ohm J, Ostermann J. GVC: efficient random access compression for gene sequence variations. BMC Bioinformatics. 2023;24(1). doi:10.1186/s12859-023-05240-0. PMID:36978010. PMCID:PMC10044409.