An Improved Chinese String Comparator for Bloom Filter Based Privacy-Preserving Record Linkage.
Siqi Sun1, Yining Qian1, Ruoshi Zhang1
1Department of Mathematics and Statistics, College of Science, Huazhong Agricultural University, Wuhan 430070, China.
Entropy (Basel, Switzerland)
|August 27, 2021
Summary
This study introduces a novel privacy-preserving record linkage (PPRL) method for Chinese data. It effectively links records without compromising privacy, improving classification accuracy with minimal computational overhead.
Area of Science:
- Computer Science
- Information Security
- Data Linkage
Background:
- Data sharing is crucial but raises privacy concerns.
- Existing privacy-preserving record linkage (PPRL) methods are primarily designed for alphabetic languages.
- Chinese language presents unique challenges for PPRL due to its character-based nature.
Purpose of the Study:
- To develop and evaluate a novel PPRL technique tailored for the Chinese language environment.
- To address the limitations of existing PPRL methods in non-alphabetic contexts.
- To enhance data linkage accuracy while ensuring privacy.
Main Methods:
- Chinese characters are encoded into SoundShape codes based on pronunciation and shape.
- SoundShape codes are encrypted using a Bloom filter.
- Record similarity is calculated using Dice similarity on encrypted fields.
- The impact of Bloom filter's false positive rate and sound/shape code proportions were analyzed.
Main Results:
- The proposed method demonstrated improved precision, recall, and F1-score on synthetic datasets.
- Performance was evaluated across various false positive rates and sound/shape code proportions.
- The approach achieved high-quality classification results for Chinese PPRL.
- The method offered a relatively low additional computational cost.
Conclusions:
- The developed SoundShape code and Bloom filter-based PPRL method is effective for Chinese language data.
- This technique successfully balances data linkage accuracy with privacy preservation.
- The findings suggest a viable solution for PPRL in non-alphabetic language environments.
Related Concept Videos
Multiple Comparison Tests
4.1K
Multiple comparison test, abbreviated as MCT, is a post hoc analysis generally performed after comparing multiple samples with one or more tests. An MCT will help identify a significantly different sample among multiple samples or a factor among multiple factors.
It would be easy to compare two samples using a significance alpha level of 0.05. In other words, there is only one sample pair to be compared. However, it would be difficult to identify a significantly different sample if the number...
It would be easy to compare two samples using a significance alpha level of 0.05. In other words, there is only one sample pair to be compared. However, it would be difficult to identify a significantly different sample if the number...
4.1K
Routh-Hurwitz Criterion II
508
In the application of the Routh-Hurwitz criterion, two specific scenarios can arise that complicate stability analysis.
The first scenario occurs when a singular zero appears in the first column of the Routh table. This situation creates a division by zero issues. To resolve this, a small positive or negative number, denoted as epsilon (∈), is substituted for the zero. The stability analysis proceeds by assuming a sign for ∈. If ∈ is positive, any sign change in the first...
The first scenario occurs when a singular zero appears in the first column of the Routh table. This situation creates a division by zero issues. To resolve this, a small positive or negative number, denoted as epsilon (∈), is substituted for the zero. The stability analysis proceeds by assuming a sign for ∈. If ∈ is positive, any sign change in the first...
508
Conservative Site-specific Recombination and Phase Variation
6.3K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
6.3K
Wilcoxon Signed-Ranks Test for Matched Pairs
244
The Wilcoxon signed-rank test for matched pairs evaluates the null hypothesis by combining the ranks of differences with their signs. It essentially tests whether the median of the differences in a population of matched pairs is zero. Since the test incorporates more information than the sign test, it generally yields more trustable conclusions. This test also does not require the data to follow a normal distribution, but two conditions must be met for it to be applicable: (1) the data must...
244
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
3.4K
Electrocyclic reactions, cycloadditions, and sigmatropic rearrangements are concerted pericyclic reactions that proceed via a cyclic transition state. These reactions are stereospecific and regioselective. The stereochemistry of the products depends on the symmetry characteristics of the interacting orbitals and the reaction conditions. Accordingly, pericyclic reactions are classified as either symmetry-allowed or symmetry-forbidden. Woodward and Hoffmann presented the selection criteria for...
3.4K
Comparing Copy Number Variations and SNPs
18.1K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
18.1K


