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Original article
Mathematical modeling of the impact of Omicron variant on the COVID-19 situation in South Korea
Jooha Oh, Catherine Apio, Taesung Park
Genomics Inform. 2022;20(2):e22.   Published online June 22, 2022
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Genetic analysis of the postsynaptic transmembrane X-linked neuroligin 3 gene in autism
Rajat Hegde, Smita Hegde, Suyamindra S. Kulkarni, Aditya Pandurangi, Pramod B. Gai, Kusal K. Das
Genomics Inform. 2021;19(4):e44.   Published online December 31, 2021
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Genetic alterations in Wnt family of genes and their putative association with head and neck squamous cell carcinoma
Jain Aditya, A. S. Smiline Girija, A. Paramasivam, J. Vijayashree Priyadharsini
Genomics Inform. 2021;19(1):e5.   Published online March 26, 2021
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Clinical genomics
Accelerating next generation sequencing data analysis: an evaluation of optimized best practices for Genome Analysis Toolkit algorithms
Karl R. Franke, Erin L. Crowgey
Genomics Inform. 2020;18(1):e10.   Published online March 31, 2020
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Original article
Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples
Sonali P. Barwe, Anilkumar Gopalakrisnapillai, Nitin Mahajan, Todd E. Druley, E. Anders Kolb, Erin L. Crowgey
Genomics Inform. 2020;18(1):e6.   Published online March 31, 2020
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Functional annotation of de novo variants from healthy individuals
Jean Lee, Sung Eun Hong
Genomics Inform. 2019;17(4):e46.   Published online December 23, 2019
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Insights of Window-Based Mechanism Approach to Visualize Composite BioData Point in Feature Spaces
Mosaab Daoud
Genomics Inform. 2019;17(1):e4.   Published online March 31, 2019
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Application Note
Integration of a Large-Scale Genetic Analysis Workbench Increases the Accessibility of a High-Performance Pathway-Based Analysis Method
Sungyoung Lee, Taesung Park
Genomics Inform. 2018;16(4):e39.   Published online December 28, 2018
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Original Article
A Universal Analysis Pipeline for Hybrid Capture-Based Targeted Sequencing Data with Unique Molecular Indexes
Min-Jung Kim, Si-Cho Kim, Young-Joon Kim
Genomics Inform. 2018;16(4):e29.   Published online December 28, 2018
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Clinical Genomics
Generation of Whole-Genome Sequencing Data for Comparing Primary and Castration-Resistant Prostate Cancer
Jong-Lyul Park, Seon-Kyu Kim, Jeong-Hwan Kim, Seok Joong Yun, Wun-Jae Kim, Won Tae Kim, Pildu Jeong, Ho Won Kang, Seon-Young Kim
Genomics Inform. 2018;16(3):71-74.   Published online September 30, 2018
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Original Article
Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants
Kyung Kim, Moon-Woo Seong, Won-Hyong Chung, Sung Sup Park, Sangseob Leem, Won Park, Jihyun Kim, KiYoung Lee, Rae Woong Park, Namshin Kim
Genomics Inform. 2015;13(2):31-39.   Published online June 30, 2015
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Application Note
MAP: Mutation Arranger for Defining Phenotype-Related Single-Nucleotide Variant
In-Pyo Baek, Yong-Bok Jeong, Seung-Hyun Jung, Yeun-Jun Chung
Genomics Inform. 2014;12(4):289-292.   Published online December 31, 2014
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Review Article
A Primer for Disease Gene Prioritization Using Next-Generation Sequencing Data
Shuoguo Wang, Jinchuan Xing
Genomics Inform. 2013;11(4):191-199.   Published online December 31, 2013
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Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases
Gerald Goh, Murim Choi
Genomics Inform. 2012;10(4):214-219.   Published online December 31, 2012
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