Genomics & Informatics

A Visualization Tool for Computational Analysis of DNA Methylation Level Using Bisulfite Sequencing Data.: Hongseok Tae; Genomics Inform. 2011;9(3):136-137.; DOI: https://doi.org/10.5808/gi.2011.9.3.136; PDF

Validation of Customized Cancer Panel for Detecting Somatic Mutations and Copy Number Alterations: Su-Hye Choi, Seung-Hyun Jung, Yeun-Jun Chung; Genomics Inform. 2017;15(4):136-141. Published online December 29, 2017; DOI: https://doi.org/10.5808/GI.2017.15.4.136
Cited By 3; Full text PubReader ePub PDF

Prediction of Genes Related to Positive Selection Using Whole-Genome Resequencing in Three Commercial Pig Breeds: HyoYoung Kim, Kelsey Caetano-Anolles, Minseok Seo, Young-jun Kwon, Seoae Cho, Kangseok Seo, Heebal Kim; Genomics Inform. 2015;13(4):137-145. Published online December 31, 2015; DOI: https://doi.org/10.5808/GI.2015.13.4.137
Cited By 4; Full text PubReader ePub PDF Supplementary Material

Detection of hydin Gene Duplication in Personal Genome Sequence Data.: Jong Il Kim, Young Seok Ju, Sheehyun Kim, Dongwan Hong, Jeong Sun Seo; Genomics Inform. 2009;7(3):159-162.; DOI: https://doi.org/10.5808/gi.2009.7.3.159; PDF

Application of Cancer Genomics to Solve Unmet Clinical Needs: Se-Hoon Lee, Sung Hoon Sim, Ji-Yeon Kim, SooJin Cha, Ahnah Song; Genomics Inform. 2013;11(4):174-179. Published online December 31, 2013; DOI: https://doi.org/10.5808/GI.2013.11.4.174
Cited By 6; Full text PubReader ePub PDF

IVAG: An Integrative Visualization Application for Various Types of Genomic Data Based on R-Shiny and the Docker Platform: Tae-Rim Lee, Jin Mo Ahn, Gyuhee Kim, Sangsoo Kim; Genomics Inform. 2017;15(4):178-182. Published online December 29, 2017; DOI: https://doi.org/10.5808/GI.2017.15.4.178
Cited By 1; Full text PubReader ePub PDF Supplementary Material

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
Cited By 7; Full text PubReader ePub PDF

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
Cited By 42; Full text PubReader ePub PDF

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
Cited By 27; Full text PubReader ePub PDF

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; Full text PubReader ePub PDF

Analysis of genome variants in dwarf soybean lines obtained in F6 derived from cross of normal parents (cultivated and wild soybean): Neha Samir Roy, Yong-Wook Ban, Hana Yoo, Rahul Vasudeo Ramekar, Eun Ju Cheong, Nam-Il Park, Jong Kuk Na, Kyong-Cheul Park, Ik-Young Choi; Genomics Inform. 2021;19(2):e19. Published online June 30, 2021; DOI: https://doi.org/10.5808/gi.21024
Cited By 2; Full text PubReader ePub PDF Supplementary Material

Genome characterization and mutation analysis of human influenza A virus in Thailand: Somruthai Rattanaburi, Vorthon Sawaswong, Pattaraporn Nimsamer, Oraphan Mayuramart, Pavaret Sivapornnukul, Ariya Khamwut, Prangwalai Chanchaem, Kritsada Kongnomnan, Nungruthai Suntronwong, Yong Poovorawan, Sunchai Payungporn; Genomics Inform. 2022;20(2):e21. Published online June 30, 2022; DOI: https://doi.org/10.5808/gi.21077
Cited By 2; Full text PubReader ePub PDF Supplementary Material

FusionScan: accurate prediction of fusion genes from RNA-Seq data: Pora Kim, Ye Eun Jang, Sanghyuk Lee; Genomics Inform. 2019;17(3):e26. Published online July 23, 2019; DOI: https://doi.org/10.5808/GI.2019.17.3.e26
Cited By 11; Full text PubReader ePub PDF

A semi-automatic cell type annotation method for single-cell RNA sequencing dataset: Wan Kim, Sung Min Yoon, Sangsoo Kim; Genomics Inform. 2020;18(3):e26. Published online September 8, 2020; DOI: https://doi.org/10.5808/GI.2020.18.3.e26; Full text PubReader ePub PDF Supplementary Material

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