Evidence map›Paper›PMID 26446135›Full record

ArticleBioinformatics (Oxford, England)2016

HEALER: homomorphic computation of ExAct Logistic rEgRession for secure rare disease variants analysis in GWAS.

Shuang Wang, Yuchen Zhang, Wenrui Dai, Kristin Lauter, Miran Kim, Yuzhe Tang, Hongkai Xiong, Xiaoqian Jiang

Abstract readEvaluation Study
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed.

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  17. A secure system for genomics clinical decision support.Journal of biomedical informatics · 2020
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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

8 authors.

Shuang WangDepartment of Biomedical Informatics, University of California, San Diego, CA 92093.
Yuchen ZhangDepartment of Biomedical Informatics, University of California, San Diego, CA 92093, Department of Electronic Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Wenrui DaiDepartment of Biomedical Informatics, University of California, San Diego, CA 92093, Department of Electronic Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Kristin LauterMicrosoft Research, San Diego, CA 92122, USA.
Miran KimSeoul National University, Seoul, 151-742, Republic of Korea and.
Yuzhe TangDepartment of Electrical Engineering and Computer Science, Syracuse University, Syracuse, NY 13244, USA.
Hongkai XiongDepartment of Electronic Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Xiaoqian JiangDepartment of Biomedical Informatics, University of California, San Diego, CA 92093.

Funding

iDASH: Integrating Data for Analysis, Anonymization, and SharingU54HL108460 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI OHNO-MACHADO, LUCILA · 2010 to 2015
$19.1M
Protection of Records: Privacy (PReP) Technology for Medical ResearchR00LM011392 · NLM · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JIANG, XIAOQIAN · 2013 to 2015
$650k
Protect Privacy of Healthcare Data in the CloudR21LM012060 · NLM · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JIANG, XIAOQIAN · 2014 to 2015
$376k
Protecting the pRivacy Of Genomes in Research StudieS (PROGRESS)K99HG008175 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WANG, SHUANG · 2014 to 2015
$100k
NHGRI NIH HHS K99 HG008175NHGRI NIH HHS K99HG008175NHLBI NIH HHS U54 HL108460NHLBI NIH HHS U54HL108460NLM NIH HHS R00 LM011392NLM NIH HHS R00LM011392NLM NIH HHS R21 LM012060NLM NIH HHS R21LM012060
6 · The paper itself

Abstract

motivationGenome-wide association studies (GWAS) have been widely used in discovering the association between genotypes and phenotypes. Human genome data contain valuable but highly sensitive information. Unprotected disclosure of such information might put individual's privacy at risk. It is important to protect human genome data. Exact logistic regression is a bias-reduction method based on a penalized likelihood to discover rare variants that are associated with disease susceptibility. We propose the HEALER framework to facilitate secure rare variants analysis with a small sample size.

resultsWe target at the algorithm design aiming at reducing the computational and storage costs to learn a homomorphic exact logistic regression model (i.e. evaluate P-values of coefficients), where the circuit depth is proportional to the logarithmic scale of data size. We evaluate the algorithm performance using rare Kawasaki Disease datasets. AVAILABILITY AND IMPLEMENTATION: Download HEALER at http://research.ucsd-dbmi.org/HEALER/ CONTACT: shw070@ucsd.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsGenetic PrivacyGenetic VariationGenome-Wide Association StudyGenome, HumanHumansMucocutaneous Lymph Node SyndromeRare Diseases

Identifiers

PMID26446135
PMCPMC4739182

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.