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"Most Download" Articles are updated quarterly. Below are Genomics Inform’s most frequently downloaded articles for the previous last months.

Original article
Comparison of the copy-neutral loss of heterozygosity identified from whole-exome sequencing data using three different tools   (88 times)
Gang-Taik Lee, Yeun-Jun Chung
Genomics Inform. 2022;20(1):e4.   Published online March 31, 2022
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Original Article
Exploration of errors in variance caused by using the first-order approximation in Mendelian randomization   (65 times)
Hakin Kim, Kunhee Kim, Buhm Han
Genomics Inform. 2022;20(1):e9.   Published online March 31, 2022
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Editorial
Editor’s introduction to this issue (G&I 20:1, 2022)   (64 times)
Taesung Park
Genomics Inform. 2022;20(1):e1.   Published online March 31, 2022
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Review article
Experimental development of the epigenomic library construction method to elucidate the epigenetic diversity and causal relationship between epigenome and transcriptome at a single-cell level   (86 times)
Kyunghyuk Park, Min Chul Jeon, Bokyung Kim, Bukyoung Cha, Jong-Il Kim
Genomics Inform. 2022;20(1):e2.   Published online March 31, 2022
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Whole-genome sequence analysis through online web interfaces: a review   (93 times)
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
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Original article
Bayesian mixed models for longitudinal genetic data: theory, concepts, and simulation studies   (71 times)
Wonil Chung, Youngkwang Cho
Genomics Inform. 2022;20(1):e8.   Published online March 31, 2022
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Hypothetical protein predicted to be tumor suppressor: a protein functional analysis   (84 times)
Md. Abdul Kader, Akash Ahammed, Md. Sharif Khan, Sheikh Abdullah Al Ashik, Md. Shariful Islam, Mohammad Uzzal Hossain
Genomics Inform. 2022;20(1):e6.   Published online March 31, 2022
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Designing a novel mRNA vaccine against Vibrio harveyi infection in fish: an immunoinformatics approach   (89 times)
Sk Injamamul Islam, Moslema Jahan Mou, Saloa Sanjida, Muhammad Tariq, Saad Nasir, Sarower Mahfuj
Genomics Inform. 2022;20(1):e11.   Published online March 31, 2022
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Presentation of potential genes and deleterious variants associated with non-syndromic hearing loss: a computational approach   (69 times)
Manisha Ray, Surya Narayan Rath, Saurav Sarkar, Mukund Namdev Sable
Genomics Inform. 2022;20(1):e5.   Published online March 31, 2022
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Publication trends of somatic mutation and recombination tests research: a bibliometric analysis (1984‒2020)   (72 times)
Ghada Tagorti, Bülent Kaya
Genomics Inform. 2022;20(1):e10.   Published online March 31, 2022
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