Genomics & Informatics

Efficiency to Discovery Transgenic Loci in GM Rice Using Next Generation Sequencing Whole Genome Re-sequencing: Doori Park, Dongin Kim, Green Jang, Jongsung Lim, Yun-Ji Shin, Jina Kim, Mi-Seong Seo, Su-Hyun Park, Ju-Kon Kim, Tae-Ho Kwon, Ik-Young Choi; Genomics Inform. 2015;13(3):81-85. Published online September 30, 2015; DOI: https://doi.org/10.5808/GI.2015.13.3.81
Cited By 14; Full text PubReader ePub PDF Supplementary Material

An Optimized Strategy for Genome Assembly of Sanger/pyrosequencing Hybrid Data using Available Software.: Haeyoung Jeong, Jihyun F Kim; Genomics Inform. 2008;6(2):87-90.; DOI: https://doi.org/10.5808/gi.2008.6.2.087; PDF

A Simple GUI-based Sequencing Format Conversion Tool for the Three NGS Platforms.: Arang Rhie, Sanduk Yang, Kyung Eun Lee, Chin Ting Thong, Hyun Seok Park; Genomics Inform. 2010;8(2):97-99.; DOI: https://doi.org/10.5808/gi.2010.8.2.097; 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 3; 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

Functional annotation of lung cancer‒associated genetic variants by cell type‒specific epigenome and long-range chromatin interactome: Andrew J. Lee, Inkyung Jung; Genomics Inform. 2021;19(1):e3. Published online March 25, 2021; DOI: https://doi.org/10.5808/gi.20073; Full text PubReader ePub PDF Supplementary Material

Whole-genome sequence analysis through online web interfaces: a review: A. W. A. C. W. R. Gunasekara, L. G. T. G. Rajapaksha, T.L. Tung; Genomics Inform. 2022;20(1):e3. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.20038
Cited By 1; Full text PubReader ePub PDF

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

PAIVS: prediction of avian influenza virus subtype: Hyeon-Chun Park, Juyoun Shin, Sung-Min Cho, Shinseok Kang, Yeun-Jun Chung, Seung-Hyun Jung; Genomics Inform. 2020;18(1):e5. Published online March 31, 2020; DOI: https://doi.org/10.5808/GI.2020.18.1.e5
Cited By 2; Full text PubReader ePub PDF Supplementary Material

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
Cited By 2; Full text PubReader ePub PDF Supplementary Material

Analytical Tools and Databases for Metagenomics in the Next-Generation Sequencing Era: Mincheol Kim, Ki-Hyun Lee, Seok-Whan Yoon, Bong-Soo Kim, Jongsik Chun, Hana Yi; Genomics Inform. 2013;11(3):102-113. Published online September 30, 2013; DOI: https://doi.org/10.5808/GI.2013.11.3.102
Cited By 74; Full text PubReader ePub PDF

Analysis of Whole Transcriptome Sequencing Data: Workflow and Software: In Seok Yang, Sangwoo Kim; Genomics Inform. 2015;13(4):119-125. Published online December 31, 2015; DOI: https://doi.org/10.5808/GI.2015.13.4.119
Cited By 35; Full text PubReader ePub PDF

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

misMM: An Integrated Pipeline for Misassembly Detection Using Genotyping-by-Sequencing and Its Validation with BAC End Library Sequences and Gene Synteny: Young-Joon Ko, Jung Sun Kim, Sangsoo Kim; Genomics Inform. 2017;15(4):128-135. Published online December 29, 2017; DOI: https://doi.org/10.5808/GI.2017.15.4.128; Full text PubReader ePub PDF

Identification of Causal and/or Rare Genetic Variants for Complex Traits by Targeted Resequencing in Population-based Cohorts.: Yun Kyoung Kim, Chang Bum Hong, Yoon Shin Cho; Genomics Inform. 2010;8(3):131-137.; DOI: https://doi.org/10.5808/gi.2010.8.3.131; PDF

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