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Next-Generation Sequencing and Epigenomics Research: A Hammer in Search of Nails
Shrutii Sarda, Sridhar Hannenhalli
Genomics Inform. 2014;12(1):2-11.   Published online March 31, 2014
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A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages
Seung-Jin Park, Jong-Hwan Kim, Byung-Ha Yoon, Seon-Young Kim
Genomics Inform. 2017;15(1):11-18.   Published online March 29, 2017
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CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics
Young-Kyu Park, Tae-Wook Kang, Su-Jin Baek, Kwon-Il Kim, Seon-Young Kim, Doheon Lee, Yong Sung Kim
Genomics Inform. 2012;10(1):33-39.   Published online March 31, 2012
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Ultra-rare Disease and Genomics-Driven Precision Medicine
Sangmoon Lee, Murim Choi
Genomics Inform. 2016;14(2):42-45.   Published online June 30, 2016
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New Lung Cancer Panel for High-Throughput Targeted Resequencing
Eun-Hye Kim, Sunghoon Lee, Jongsun Park, Kyusang Lee, Jong Bhak, Byung Chul Kim
Genomics Inform. 2014;12(2):50-57.   Published online June 30, 2014
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Current Challenges in Bacterial Transcriptomics
Suhyung Cho, Yoobok Cho, Sooin Lee, Jayoung Kim, Hyeji Yum, Sun Chang Kim, Byung-Kwan Cho
Genomics Inform. 2013;11(2):76-82.   Published online June 30, 2013
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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
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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
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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
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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
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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
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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
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A genetic approach to comprehend the complex and dynamic event of floral development: a review
Jatindra Nath Mohanty, Swayamprabha Sahoo, Puspanjali Mishra
Genomics Inform. 2022;20(4):e40.   Published online December 30, 2022
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Development of an RNA sequencing panel to detect gene fusions in thyroid cancer
Dongmoung Kim, Seung-Hyun Jung, Yeun-Jun Chung
Genomics Inform. 2021;19(4):e41.   Published online December 31, 2021
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Detection of KRAS mutations in plasma cell-free DNA of colorectal cancer patients and comparison with cancer panel data for tissue samples of the same cancers
Suji Min, Sun Shin, Yeun-Jun Chung
Genomics Inform. 2019;17(4):e42.   Published online November 29, 2019
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