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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; DOI: https://doi.org/10.5808/GI.2015.13.2.31
Cited By 10; Full text PubReader ePub PDF Supplementary Material

Genetic Risk Prediction for Normal-Karyotype Acute Myeloid Leukemia Using Whole-Exome Sequencing: Seong Gu Heo, Eun Pyo Hong, Ji Wan Park; Genomics Inform. 2013;11(1):46-51. Published online March 31, 2013; DOI: https://doi.org/10.5808/GI.2013.11.1.46
Cited By 6; Full text PubReader ePub PDF

Recent Progress of Genome Study for Anaplastic Thyroid Cancer: Jieun Lee, Jung-Ah Hwang, Eun Kyung Lee; Genomics Inform. 2013;11(2):68-75. Published online June 30, 2013; DOI: https://doi.org/10.5808/GI.2013.11.2.68
Cited By 19; Full text PubReader ePub PDF

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
Cited By 3; Full text PubReader ePub PDF

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
Cited By 2; Full text PubReader ePub PDF

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