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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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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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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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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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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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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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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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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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Generation and analysis of whole-genome sequencing data in human mammary epithelial cells
Jong-Lyul Park, Jae-Yoon Kim, Seon-Young Kim, Yong Sun Lee
Genomics Inform. 2023;21(1):e11.   Published online March 31, 2023
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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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A bioinformatic approach to identify pathogenic variants for Stevens-Johnson syndrome
Muhammad Ma’ruf, Justitia Cahyani Fadli, Muhammad Reza Mahendra, Lalu Muhammad Irham, Nanik Sulistyani, Wirawan Adikusuma, Rockie Chong, Abdi Wira Septama
Genomics Inform. 2023;21(2):e26.   Published online June 30, 2023
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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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Identification of druggable genes for multiple myeloma based on genomic information
Rahmat Dani Satria, Lalu Muhammad Irham, Wirawan Adikusuma, Anisa Nova Puspitaningrum, Arief Rahman Afief, Riat El Khair, Abdi Wira Septama
Genomics Inform. 2023;21(3):e31.   Published online September 27, 2023
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Identifying pathogenic variants related to systemic lupus erythematosus by integrating genomic databases and a bioinformatic approach
Ratih Dewi Yudhani, Dyonisa Nasirochmi Pakha, Suyatmi Suyatmi, Lalu Muhammad Irham
Genomics Inform. 2023;21(3):e37.   Published online September 27, 2023
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