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

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 (559 times): Kyunghyuk Park, Min Chul Jeon, Bokyung Kim, Bukyoung Cha, Jong-Il Kim; Genomics Inform. 2022;20(1):e2. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.21078; Full text PubReader ePub Crossref - TDM PDF

Whole-genome sequence analysis through online web interfaces: a review (576 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; DOI: https://doi.org/10.5808/gi.20038; Full text PubReader ePub Crossref - TDM PDF

Genome archive
Characterization of the first mitogenomes of the smallest fish in the world, Paedocypris progenetica, from peat swamp of Peninsular Malaysia, Selangor, and Perak (513 times): NorJasmin Hussin, Izzati Adilah Azmir, Yuzine Esa, Amirrudin Ahmad, Faezah Mohd Salleh, Puteri Nur Syahzanani Jahari, Kaviarasu Munian, Han Ming Gan; Genomics Inform. 2022;20(1):e12. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.21081; Full text PubReader ePub Crossref - TDM PDF

Original article
Molecular characterization and functional annotation of a hypothetical protein (SCO0618) of Streptomyces coelicolor A3(2) (4,392 times): Nadim Ferdous, Mahjerin Nasrin Reza, Md. Tabassum Hossain Emon, Md. Shariful Islam, A. K. M Mohiuddin, Mohammad Uzzal Hossain; Genomics Inform. 2020;18(3):e28. Published online September 21, 2020; DOI: https://doi.org/10.5808/GI.2020.18.3.e28
Cited By 5; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Spike protein D614G and RdRp P323L: the SARS-CoV-2 mutations associated with severity of COVID-19 (3,575 times): Subrata K. Biswas, Sonchita R. Mudi; Genomics Inform. 2020;18(4):e44. Published online December 7, 2020; DOI: https://doi.org/10.5808/GI.2020.18.4.e44
Cited By 17; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Designing a novel mRNA vaccine against Vibrio harveyi infection in fish: an immunoinformatics approach (517 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; DOI: https://doi.org/10.5808/gi.21065
Cited By 1; Full text PubReader ePub Crossref - TDM PDF

Application note
Social Media Mining Toolkit (SMMT) (8,496 times): Ramya Tekumalla, Juan M. Banda; Genomics Inform. 2020;18(2):e16. Published online June 15, 2020; DOI: https://doi.org/10.5808/GI.2020.18.2.e16
Cited By 8; Full text PubReader ePub Crossref - TDM PDF

Original article
Potential biomarkers and signaling pathways associated with the pathogenesis of primary salivary gland carcinoma: a bioinformatics study (1,080 times): Zeynab Bayat, Fatemeh Ahmadi-Motamayel, Mohadeseh Salimi Parsa, Amir Taherkhani; Genomics Inform. 2021;19(4):e42. Published online December 31, 2021; DOI: https://doi.org/10.5808/gi.21052; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Editorial
Editor’s introduction to this issue (G&I 20:1, 2022) (376 times): Taesung Park; Genomics Inform. 2022;20(1):e1. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.20.1.e1; Full text PubReader ePub Crossref - TDM PDF

Original article
Comparison of the copy-neutral loss of heterozygosity identified from whole-exome sequencing data using three different tools (488 times): 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; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Comparative analysis of commonly used peak calling programs for ChIP-Seq analysis (2,978 times): Hyeongrin Jeon, Hyunji Lee, Byunghee Kang, Insoon Jang, Tae-Young Roh; Genomics Inform. 2020;18(4):e42. Published online December 14, 2020; DOI: https://doi.org/10.5808/GI.2020.18.4.e42
Cited By 3; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Publication trends of somatic mutation and recombination tests research: a bibliometric analysis (1984‒2020) (418 times): Ghada Tagorti, Bülent Kaya; Genomics Inform. 2022;20(1):e10. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.21083; Full text PubReader ePub Crossref - TDM PDF

Genome archive
Sequencing and annotation of the complete mitochondrial genome of a threatened labeonine fish, Cirrhinus reba (2,839 times): Mohammad Nazrul Islam, Shirin Sultana, Md. Jobaidul Alam; Genomics Inform. 2020;18(3):e32. Published online September 10, 2020; DOI: https://doi.org/10.5808/GI.2020.18.3.e32
Cited By 2; Full text PubReader ePub Crossref - TDM PDF

Original article
Bayesian mixed models for longitudinal genetic data: theory, concepts, and simulation studies (391 times): Wonil Chung, Youngkwang Cho; Genomics Inform. 2022;20(1):e8. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.21080; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

In-silico characterization and structure-based functional annotation of a hypothetical protein from Campylobacter jejuni involved in propionate catabolism (1,151 times): Lincon Mazumder, Mehedi Hasan, Ahmed Abu Rus'd, Mohammad Ariful Islam; Genomics Inform. 2021;19(4):e43. Published online December 31, 2021; DOI: https://doi.org/10.5808/gi.21043; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Application note
MPI-GWAS: a supercomputing-aided permutation approach for genomewide association studies (381 times): Hyojung Paik, Yongseong Cho, Seong Beom Cho, Oh-Kyoung Kwon; Genomics Inform. 2022;20(1):e14. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.22001; Full text PubReader Crossref - TDM PDF

Original article
Presentation of potential genes and deleterious variants associated with non-syndromic hearing loss: a computational approach (381 times): Manisha Ray, Surya Narayan Rath, Saurav Sarkar, Mukund Namdev Sable; Genomics Inform. 2022;20(1):e5. Published online March 31, 2022; DOI: https://doi.org/10.5808/gi.21070; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Clinical genomics
Accelerating next generation sequencing data analysis: an evaluation of optimized best practices for Genome Analysis Toolkit algorithms (3,616 times): Karl R. Franke, Erin L. Crowgey; Genomics Inform. 2020;18(1):e10. Published online March 31, 2020; DOI: https://doi.org/10.5808/GI.2020.18.1.e10
Cited By 6; Full text PubReader ePub Crossref - TDM PDF

Original article
Analysis of H3K4me3-ChIP-Seq and RNA-Seq data to understand the putative role of miRNAs and their target genes in breast cancer cell lines (2,220 times): Aneesh Kotipalli, Ruma Banerjee, Sunitha Manjari Kasibhatla, Rajendra Joshi; Genomics Inform. 2021;19(2):e17. Published online June 30, 2021; DOI: https://doi.org/10.5808/gi.21020; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

Identification of rare coding variants associated with Kawasaki disease by whole exome sequencing (1,077 times): Jae-Jung Kim, Young Mi Hong, Sin Weon Yun, Kyung-Yil Lee, Kyung Lim Yoon, Myung-Ki Han, Gi Beom Kim, Hong-Ryang Kil, Min Seob Song, Hyoung Doo Lee, Kee Soo Ha, Hyun Ok Jun, Byung-Ok Choi, Yeon-Mok Oh, Jeong Jin Yu, Gi Young Jang, Jong-Keuk Lee; Genomics Inform. 2021;19(4):e38. Published online December 31, 2021; DOI: https://doi.org/10.5808/gi.21046; Full text PubReader ePub Crossref - TDM PDF

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Tel: +82-2-558-9394 Fax: +82-2-558-9434 E-mail: kogo3@kogo.or.kr

Copyright © 2022 by Korea Genome Organization.

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