Eliora Violain Buyamin

ORCID: 0009-0003-4557-8420
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About
Contact & Profiles
Research Areas
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • Single-cell and spatial transcriptomics
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Immune responses and vaccinations
  • CRISPR and Genetic Engineering
  • RNA Research and Splicing
  • Cell Adhesion Molecules Research

Agency for Science, Technology and Research
2023-2025

Genome Institute of Singapore
2023-2025

Summary Lack of diversity and proportionate representation in genomics datasets databases contributes to inequity healthcare outcomes globally 1,2 . The relationships human with biological biomedical phenotypes are pervasive 3 , yet remain understudied, particularly a single-cell context. Here we present the Asian Immune Diversity Atlas (AIDA), multi-national RNA-sequencing (scRNA-seq) healthy reference atlas immune cells. AIDA comprises 1,265,624 circulating cells from 619 donors 6...

10.1101/2024.06.30.601119 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-07-01
Yoshihiko Tomofuji Ryuya Edahiro Kyuto Sonehara Yuya Shirai Kian Hong Kock and 95 more Qingbo Wang Shinichi Namba Jonathan Moody Yoshinari Ando Akari Suzuki Tomohiro Yata Kotaro Ogawa Tatsuhiko Naito Ho Namkoong Quy Xiao Xuan Lin Eliora Violain Buyamin Le Min Tan Radhika Sonthalia Kyung Yeon Han Hiromu Tanaka Ho Lee Varodom Charoensawan Chung-Chau Hon Partha P. Majumder Ponpan Matangkasombut Woong‐Yang Park Shyam Prabhakar Jay W. Shin Piero Carninci John C. Chambers Marie Loh Manop Pithukpakorn Bhoom Suktitipat Kazuhiko Yamamoto Deepa Rajagopalan Nirmala Arul Rayan Shvetha Sankaran Juthamard Chantaraamporn Ankita Chatterjee Supratim Ghosh Kyung Yeon Han Damita Jevapatarakul Sarintip Nguantad Sumanta Sarkar Narita Thungsatianpun Mai Abe Seiko Furukawa Gyo Inoue Keiko Myouzen Jin‐Mi Oh Akari Suzuki Yoshinari Ando Miki Kojima Tsukasa Kouno Jinyeong Lim Arindam Maitra Le Min Tan Prasanna Nori Venkatesh Murim Choi Jong‐Eun Park Eliora Violain Buyamin Kian Hong Kock Quy Xiao Xuan Lin Jonathan Moody Radhika Sonthalia Kazuyoshi Ishigaki Masahiro Nakano Yukinori Okada Yoshihiko Tomofuji Ho Namkoong Ryuya Edahiro Tomomi Takano Hiroshi Nishihara Yuya Shirai Kyuto Sonehara Hiromu Tanaka Shuhei Azekawa Yohei Mikami Ho Lee Takanori Hasegawa Koji Okudela Daisuke Okuzaki Daisuke Motooka Masahiro Kanai Tatsuhiko Naito Kenichi Yamamoto Qingbo Wang Ryunosuke Saiki Rino Ishihara Yuta Matsubara Junko Hamamoto Hiroyuki Hayashi Yukihiro Yoshimura Natsuo Tachikawa Emmy Yanagita Takayoshi Hyugaji Eigo Shimizu Kotoe Katayama Yasuhiro Kato Takayoshi Morita

Several X-linked genes escape from X chromosome inactivation (XCI), while differences in across cell types and tissues are still poorly characterized. Here, we developed scLinaX for directly quantifying relative gene expression the inactivated with droplet-based single-cell RNA sequencing (scRNA-seq) data. The differentially expressed analyses large-scale blood scRNA-seq datasets consistently identified stronger lymphocytes than myeloid cells. An extension of to a 10x multiome dataset...

10.1016/j.xgen.2024.100625 article EN cc-by-nc-nd Cell Genomics 2024-07-30

Alternative splicing contributes to complex traits, but whether this differs in trait-relevant cell types across diverse genetic ancestries is unclear. Here we describe cell-type-specific, sex-biased and ancestry-biased alternative ~1 M peripheral blood mononuclear cells from 474 healthy donors the Asian Immune Diversity Atlas. We identify widespread differential splicing, most of which cell-type-specific. 11,577 independent cis-splicing quantitative trait loci (sQTLs), 607 trans-sGenes 107...

10.1038/s41588-024-02019-8 article EN cc-by-nc-nd Nature Genetics 2024-12-01

Abstract One of the two X chromosomes females is silenced through chromosome inactivation (XCI) to compensate for difference in dosage between sexes. Among X-linked genes, several genes escape from XCI, which could contribute differential gene expression However, differences across cell types and tissues are still poorly characterized because no methods directly evaluate under a physiological condition at cell-cluster resolution with versatile technology. Here, we developed method, s ingle-...

10.1101/2023.10.14.561800 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2023-10-18
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