Genomics & Informatics

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; DOI: https://doi.org/10.5808/GI.2015.13.2.31
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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; DOI: https://doi.org/10.5808/GI.2018.16.3.71
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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; DOI: https://doi.org/10.5808/GI.2019.17.1.e4
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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; DOI: https://doi.org/10.5808/gi.20065
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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; DOI: https://doi.org/10.5808/GI.2020.18.1.e6
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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; DOI: https://doi.org/10.5808/GI.2013.11.4.191
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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; DOI: https://doi.org/10.5808/GI.2012.10.4.214
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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; DOI: https://doi.org/10.5808/GI.2014.12.4.289; Full text PubReader ePub PDF

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; DOI: https://doi.org/10.5808/GI.2020.18.1.e10
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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; DOI: https://doi.org/10.5808/gi.22044
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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; DOI: https://doi.org/10.5808/gi.22025
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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; DOI: https://doi.org/10.5808/gi.23010
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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; DOI: https://doi.org/10.5808/GI.2018.16.4.e29
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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; DOI: https://doi.org/10.5808/gi.23011
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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; DOI: https://doi.org/10.5808/gi.23002
Cited By 4; Full text PubReader ePub PDF

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