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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
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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
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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
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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
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