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Author Details

Soohyun Lee
2004
36
22
PMIDPaper TitleJournal TitlePublished Year
34415533Hi-C Data Formats.Methods in Molecular Biology2022
35501320The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.Nat Commun2022
36323678Author Correction: The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.Nat Commun2022
34838103Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder.Mob DNA2021
34158502Comprehensive identification of transposable element insertions using multiple sequencing technologies.Nat Commun2021
34189515Withdrawal: Update physical genomic information for commercial bovine SNP chip based on recent reference genome sequences (ARS-UCD1.2).Journal of Animal Science and Technology2021
33136153HiTea: a computational pipeline to identify non-reference transposable element insertions in Hi-C data.Bioinformatics2021
33416869BamSnap: a lightweight viewer for sequencing reads in BAM files.Bioinformatics2021
30686754Loss of SLC25A11 causes suppression of NSCLC and melanoma tumor formation.eBioMedicine2019
31077294Tibanna: software for scalable execution of portable pipelines on the cloud.Bioinformatics2019
30463244Renal Cell Carcinoma Is Abrogated by p53 Stabilization through Transglutaminase 2 Inhibition.Cancers2018
30356107Targeting Mitochondrial Oxidative Phosphorylation Abrogated Irinotecan Resistance in NSCLC.Scientific Reports2018
30143029HiGlass: web-based visual exploration and analysis of genome interaction maps.Genome Biol2018
29988410Functional Partitioning of Genomic Variance and Genome-Wide Association Study for Carcass Traits in Korean Hanwoo Cattle Using Imputed Sequence Level SNP Data.Frontiers in Genetics2018
29898899Linking transcriptional and genetic tumor heterogeneity through allele analysis of single-cell RNA-seq data.Genome Res2018
28366588DUSP9 Modulates DNA Hypomethylation in Female Mouse Pluripotent Stem Cells.Cell Stem Cell2017
28369524NGSCheckMate: software for validating sample identity in next-generation sequencing studies within and across data types.Nucleic Acids Res2017
26675720Corrigendum: Failure to replicate the STAP cell phenomenon.Nature2016
27153396Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome Sequencing.Am J Hum Genet2016
26675727Corrigendum: Hallmarks of pluripotency.Nature2016
26335049EMSAR: estimation of transcript abundance from RNA-seq data by mappability-based segmentation and reclustering.BMC Bioinformatics2015
26399835Failure to replicate the STAP cell phenomenon.Nature2015
26399828Hallmarks of pluripotency.Nature2015
26430121Somatic mutation in single human neurons tracks developmental and transcriptional history.Science2015
26501951A comparison of genetically matched cell lines reveals the equivalence of human iPSCs and ESCs.Nat Biotechnol2015
25164756Comparative analysis of metazoan chromatin organization.Nature2014
22927429Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution.Proceedings of the National Academy of Sciences of the United States of America2012
21059678Accurate quantification of transcriptome from RNA-Seq data by effective length normalization.Nucleic Acids Research2011
20535230Relative codon adaptation index, a sensitive measure of codon usage bias.Evolutionary Bioinformatics2010
19395009Collapse of germline piRNAs in the absence of Argonaute3 reveals somatic piRNAs in flies.Cell2009
19732946The Drosophila HP1 homolog Rhino is required for transposon silencing and piRNA production by dual-strand clusters.Cell2009
18403677Endogenous siRNAs derived from transposons and mRNAs in Drosophila somatic cells.Science2008
19093001Quantitative analysis of single nucleotide polymorphisms within copy number variation.PLoS One2008
16700068The complete genome sequence of a dog: a perspective.Bioessays2006
16309559Genes involved in complex adaptive processes tend to have highly conserved upstream regions in mammalian genomes.BMC Genomics2005
14764562CHOISS for selection of single nucleotide polymorphism markers on interval regularity.Bioinformatics2004
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