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
Cited By 11; Full text PubReader ePub PDF Supplementary Material

Ultra-rare Disease and Genomics-Driven Precision Medicine: Sangmoon Lee, Murim Choi; Genomics Inform. 2016;14(2):42-45. Published online June 30, 2016; DOI: https://doi.org/10.5808/GI.2016.14.2.42
Cited By 6; Full text PubReader ePub PDF

Elucidating molecular mechanisms of acquired resistance to BRAF inhibitors in melanoma using a microfluidic device and deep sequencing: Jiyeon Han, Yeonjoo Jung, Yukyung Jun, Sungsu Park, Sanghyuk Lee; Genomics Inform. 2021;19(1):e2. Published online March 15, 2021; DOI: https://doi.org/10.5808/gi.20074
Cited By 4; Full text PubReader ePub PDF Supplementary Material

Validity of patient-derived xenograft mouse models for lung cancer based on exome sequencing data: Jaewon Kim, Hwanseok Rhee, Jhingook Kim, Sanghyuk Lee; Genomics Inform. 2020;18(1):e3. Published online March 31, 2020; DOI: https://doi.org/10.5808/GI.2020.18.1.e3
Cited By 5; Full text PubReader ePub PDF Supplementary Material

Comparison of the copy-neutral loss of heterozygosity identified from whole-exome sequencing data using three different tools: Gang-Taik Lee, Yeun-Jun Chung; Genomics Inform. 2022;20(1):e4. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.21066
Cited By 2; Full text PubReader ePub PDF Supplementary Material

Association of HLA Genotype and Fulminant Type 1 Diabetes in Koreans: Soo Heon Kwak, Yoon Ji Kim, Jeesoo Chae, Cue Hyunkyu Lee, Buhm Han, Jong-Il Kim, Hye Seung Jung, Young Min Cho, Kyong Soo Park; Genomics Inform. 2015;13(4):126-131. Published online December 31, 2015; DOI: https://doi.org/10.5808/GI.2015.13.4.126
Cited By 13; 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 45; Full text PubReader ePub PDF

Whole-exome sequencing analysis in a case of primary congenital glaucoma due to the partial uniparental isodisomy: Parisima Ghaffarian Zavarzadeh, Morteza Bonyadi, Zahra Abedi; Genomics Inform. 2022;20(3):e28. Published online September 30, 2022; DOI: https://doi.org/10.5808/gi.21044
Cited By 2; Full text PubReader ePub PDF

Two novel mutations in ALDH18A1 and SPG11 gene found by whole-exome sequencing in spastic paraplegia disease patients in Iran: Sajad Rafiee Komachali, Zakieh Siahpoosh, Mansoor Salehi; Genomics Inform. 2022;20(3):e30. Published online September 30, 2022; DOI: https://doi.org/10.5808/gi.22030; Full text PubReader ePub PDF

Somatic Mutations from Whole Exome Sequencing Analysis of the Patients with Biliary Tract Cancer: Kyong-Ah Yoon, Sang Myung Woo, Yun-Hee Kim, Sun-Young Kong, Sung-Sik Han, Sang-Jae Park, Woo Jin Lee; Genomics Inform. 2018;16(4):e35. Published online December 28, 2018; DOI: https://doi.org/10.5808/GI.2018.16.4.e35
Cited By 3; Full text PubReader ePub PDF Supplementary Material

Identification of rare coding variants associated with Kawasaki disease by whole exome sequencing: Jae-Jung Kim, Young Mi Hong, Sin Weon Yun, Kyung-Yil Lee, Kyung Lim Yoon, Myung-Ki Han, Gi Beom Kim, Hong-Ryang Kil, Min Seob Song, Hyoung Doo Lee, Kee Soo Ha, Hyun Ok Jun, Byung-Ok Choi, Yeon-Mok Oh, Jeong Jin Yu, Gi Young Jang, Jong-Keuk Lee; Genomics Inform. 2021;19(4):e38. Published online December 31, 2021; DOI: https://doi.org/10.5808/gi.21046
Cited By 2; Full text PubReader ePub PDF

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