Skip to Main Content
CKG
Home
Home
Home
TKG
Author details
Breadcrumb
Author Details
Full Name
Soohyun Lee
Affiliation
ORCID
Career Start Year
2004
Papers
36
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34415533
Hi-C Data Formats.
Methods in Molecular Biology
2022
35501320
The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.
Nat Commun
2022
36323678
Author Correction: The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.
Nat Commun
2022
34838103
Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder.
Mob DNA
2021
34158502
Comprehensive identification of transposable element insertions using multiple sequencing technologies.
Nat Commun
2021
34189515
Withdrawal: Update physical genomic information for commercial bovine SNP chip based on recent reference genome sequences (ARS-UCD1.2).
Journal of Animal Science and Technology
2021
33136153
HiTea: a computational pipeline to identify non-reference transposable element insertions in Hi-C data.
Bioinformatics
2021
33416869
BamSnap: a lightweight viewer for sequencing reads in BAM files.
Bioinformatics
2021
30686754
Loss of SLC25A11 causes suppression of NSCLC and melanoma tumor formation.
eBioMedicine
2019
31077294
Tibanna: software for scalable execution of portable pipelines on the cloud.
Bioinformatics
2019
30463244
Renal Cell Carcinoma Is Abrogated by p53 Stabilization through Transglutaminase 2 Inhibition.
Cancers
2018
30356107
Targeting Mitochondrial Oxidative Phosphorylation Abrogated Irinotecan Resistance in NSCLC.
Scientific Reports
2018
30143029
HiGlass: web-based visual exploration and analysis of genome interaction maps.
Genome Biol
2018
29988410
Functional Partitioning of Genomic Variance and Genome-Wide Association Study for Carcass Traits in Korean Hanwoo Cattle Using Imputed Sequence Level SNP Data.
Frontiers in Genetics
2018
29898899
Linking transcriptional and genetic tumor heterogeneity through allele analysis of single-cell RNA-seq data.
Genome Res
2018
28366588
DUSP9 Modulates DNA Hypomethylation in Female Mouse Pluripotent Stem Cells.
Cell Stem Cell
2017
28369524
NGSCheckMate: software for validating sample identity in next-generation sequencing studies within and across data types.
Nucleic Acids Res
2017
26675720
Corrigendum: Failure to replicate the STAP cell phenomenon.
Nature
2016
27153396
Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome Sequencing.
Am J Hum Genet
2016
26675727
Corrigendum: Hallmarks of pluripotency.
Nature
2016
26335049
EMSAR: estimation of transcript abundance from RNA-seq data by mappability-based segmentation and reclustering.
BMC Bioinformatics
2015
26399835
Failure to replicate the STAP cell phenomenon.
Nature
2015
26399828
Hallmarks of pluripotency.
Nature
2015
26430121
Somatic mutation in single human neurons tracks developmental and transcriptional history.
Science
2015
26501951
A comparison of genetically matched cell lines reveals the equivalence of human iPSCs and ESCs.
Nat Biotechnol
2015
25164756
Comparative analysis of metazoan chromatin organization.
Nature
2014
22927429
Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution.
Proceedings of the National Academy of Sciences of the United States of America
2012
21059678
Accurate quantification of transcriptome from RNA-Seq data by effective length normalization.
Nucleic Acids Research
2011
20535230
Relative codon adaptation index, a sensitive measure of codon usage bias.
Evolutionary Bioinformatics
2010
19395009
Collapse of germline piRNAs in the absence of Argonaute3 reveals somatic piRNAs in flies.
Cell
2009
19732946
The Drosophila HP1 homolog Rhino is required for transposon silencing and piRNA production by dual-strand clusters.
Cell
2009
18403677
Endogenous siRNAs derived from transposons and mRNAs in Drosophila somatic cells.
Science
2008
19093001
Quantitative analysis of single nucleotide polymorphisms within copy number variation.
PLoS One
2008
16700068
The complete genome sequence of a dog: a perspective.
Bioessays
2006
16309559
Genes involved in complex adaptive processes tend to have highly conserved upstream regions in mammalian genomes.
BMC Genomics
2005
14764562
CHOISS for selection of single nucleotide polymorphism markers on interval regularity.
Bioinformatics
2004
1 - 36 of 36
Column Actions
Search
Recommended Authors
Collaborators
Peter J Park
Harvard Medical School
Co-authored papers
20
Burak H Alver
Co-authored papers
7
Francesco Ferrari
Co-authored papers
6
Konrad Hochedlinger
Co-authored papers
6
Zhiping Weng
University of Massachusetts Medical School
Co-authored papers
4
Nils Gehlenborg
Harvard Medical School
Co-authored papers
4
George Q Daley
Boston Children's Hospital, Harvard Medical School
Co-authored papers
4
Semin Lee
Ulsan National Institute of Science and Technology (UNIST)
Co-authored papers
4
Alejandro De Los Angeles
Massachusetts Institute of Technology
Co-authored papers
4
Nils Gehlenborg
Co-authored papers
4
Peter Kerpedjiev
Co-authored papers
3
Chengjian Li
Co-authored papers
3
Leonid A Mirny
Co-authored papers
3
Hervé Seitz
Co-authored papers
3
Jia Xu
Co-authored papers
3
Carl Vitzthum
Co-authored papers
3
Woong-Yang Park
Samsung Genome Institute, Samsung Medical Center
Co-authored papers
3
Nezar Abdennur
Co-authored papers
3
Phillip D Zamore
Co-authored papers
3
Koray Kirli
Co-authored papers
3
Simon Kasif
Boston University
Co-authored papers
3
William E Theurkauf
Co-authored papers
2
Janet Rossant
The Hospital for Sick Children
Co-authored papers
2
Stuart H Orkin
Boston Children's Hospital and Dana-Farber Cancer Institute, Harvard Medical School
Co-authored papers
2
Maria L Zapp
Co-authored papers
2
Ellen L W Kittler
Co-authored papers
2
Sarah B Reiff
Co-authored papers
2
Carla Klattenhoff
Co-authored papers
2
Christopher A Walsh
Broad Institute of MIT and Harvard
Co-authored papers
2
Psalm Haseley
Co-authored papers
2
1 - 30