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- Comparison of the copy-neutral loss of heterozygosity identified from whole-exome sequencing data using three different tools
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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
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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
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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
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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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