Evidence map›Paper›PMID 28786362›Full record

ArticleBMC medical genomics2017

Secure approximation of edit distance on genomic data.

Md Momin Al Aziz, Dima Alhadidi, Noman Mohammed

Abstract read
In one paragraph

Article in BMC medical genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Md Momin Al AzizDepartment of Computer Science, University of Manitoba, Winnipeg, Canada. azizmma@cs.umanitoba.ca.
Dima AlhadidiZayed University, Dubai, United Arab Emirates.
Noman MohammedDepartment of Computer Science, University of Manitoba, Winnipeg, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEdit distance is a well established metric to quantify how dissimilar two strings are by counting the minimum number of operations required to transform one string into the other. It is utilized in the domain of human genomic sequence similarity as it captures the requirements and leads to a better diagnosis of diseases. However, in addition to the computational complexity due to the large genomic sequence length, the privacy of these sequences are highly important. As these genomic sequences are unique and can identify an individual, these cannot be shared in a plaintext.

methodsIn this paper, we propose two different approximation methods to securely compute the edit distance among genomic sequences. We use shingling, private set intersection methods, the banded alignment algorithm, and garbled circuits to implement these methods. We experimentally evaluate these methods and discuss both advantages and limitations.

resultsExperimental results show that our first approximation method is fast and achieves similar accuracy compared to existing techniques. However, for longer genomic sequences, both the existing techniques and our proposed first method are unable to achieve a good accuracy. On the other hand, our second approximation method is able to achieve higher accuracy on such datasets. However, the second method is relatively slower than the first proposed method.

conclusionThe proposed algorithms are generally accurate, time-efficient and can be applied individually and jointly as they have complimentary properties (runtime vs. accuracy) on different types of datasets.

Indexed as

Computer SecurityGenomicsAlgorithmsSequence AlignmentEdit distance approximation on genomic dataGenomic sequence similarityPrivacy of genomic dataSecure edit distanceSecure genomic sequence similarity

Identifiers

PMID28786362
PMCPMC5547448

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.