Hyun Min Kang
University of Michigan
H-index: 78
North America-United States
Top articles of Hyun Min Kang
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Seq-Scope Protocol: Repurposing Illumina Sequencing Flow Cells for High-Resolution Spatial Transcriptomics | bioRxiv | Yongsung Kim Weiqiu Cheng Chun-Seok Cho Yongha Hwang Yichen Si | 2024 |
High-Resolution Spatial Transcriptomic Atlas of Mouse Soleus Muscle: Unveiling Single Cell and Subcellular Heterogeneity in Health and Denervation | bioRxiv | Jer-En Hsu Lloyd Ruiz Yongha Hwang Steve Guzman Chun-Seok Cho | 2024 |
Accurate cross-platform GWAS analysis via two-stage imputation | medRxiv | Anya Greenberg Kaylia Reynolds Michelle T McNulty Matthew G Sampson Hyun Min Kang | 2024 |
SiftCell: A robust framework to detect and isolate cell-containing droplets from single-cell RNA sequence reads | Cell Systems | Jingyue Xi Sung Rye Park Jun Hee Lee Hyun Min Kang | 2023/7/19 |
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes | Nature genetics | Wouter van Rheenen Rick AA van der Spek Mark K Bakker Joke JFA van Vugt Paul J Hop | 2022/3 |
Rare coding variants in CHRNB2 reduce the likelihood of smoking | Nature Genetics | Veera M Rajagopal Kyoko Watanabe Joelle Mbatchou Ariane Ayer Peter Quon | 2023/7 |
Joint testing of rare variant burden scores using non-negative least squares | bioRxiv | Andrey Ziyatdinov Joelle Mbatchou Anthony Marcketta Joshua Backman Sheila Gaynor | 2023/2/22 |
A deep catalog of protein-coding variation in 985,830 individuals | bioRxiv | Kathie Y Sun Xiaodong Bai Siying Chen Suying Bao Manav Kapoor | 2023/5/10 |
Structural variation across 138,134 samples in the TOPMed consortium | bioRxiv | Goo Jun Adam C English Ginger A Metcalf Jianzhi Yang Mark JP Chaisson | 2023/1/25 |
Rare Variants In Hematopoietic Stem Cells (HSC) And Hematopoietic Progenitor Cells (HPC) Associated With Somatic Alterations Of The Blood | 2023/11/30 | ||
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis | Nature | Joshua S Weinstock Jayakrishnan Gopakumar Bala Bharathi Burugula Md Mesbah Uddin Nikolaus Jahn | 2023/4/27 |
FICTURE: Scalable segmentation-free analysis of submicron resolution spatial transcriptomics | bioRxiv | Yichen Si ChangHee Lee Yongha Hwang Jeong H Yun Weiqiu Cheng | 2023/11/7 |
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes | Science advances | Joshua S Weinstock Cecelia A Laurie Jai G Broome Kent D Taylor Xiuqing Guo | 2023/4/26 |
Plasma proteomic associations with genetics and health in the UK Biobank | Nature | Benjamin B Sun Joshua Chiou Matthew Traylor Christian Benner Yi-Hsiang Hsu | 2023/10/12 |
Inferring CpG methylation signatures accumulated along human history from genetic variation catalogs | bioRxiv | Yichen Si Sebastian Zöllner | 2023/3/25 |
FIVEx: an interactive eQTL browser across public datasets | Bioinformatics | Alan Kwong Andrew P Boughton Mukai Wang Peter VandeHaar Michael Boehnke | 2022/1/15 |
Germline Mutations in CIDEB and Protection against Liver Disease | New England Journal of Medicine | Niek Verweij Mary E Haas Jonas B Nielsen Olukayode A Sosina Minhee Kim | 2022/7/28 |
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes | Hindy George Peter Dornbos Mark D Chaffin Dajiang J Liu Minxian Wang | 2022/1/6 | |
Genetic regulation of the human plasma proteome in 54,306 UK Biobank participants | BioRxiv | Benjamin B Sun Joshua Chiou Matthew Traylor Christian Benner Yi-Hsiang Hsu | 2022/6/18 |
STtools: a comprehensive software pipeline for ultra-high-resolution spatial transcriptomics data | Bioinformatics advances | Jingyue Xi Jun Hee Lee Hyun Min Kang Goo Jun | 2022/1/1 |
Co-Authors
