Identification of Tumor-Specific Single-Nucleotide Variants and Intratumor Heterogeneity in LUADs by Full Length ScRNAseq

被引:0
|
作者
Marignani, P. [1 ]
Kim, J. H. [1 ]
机构
[1] Dalhousie Univ, Halifax, NS, Canada
关键词
novel; single-nucleotide variants; Full-length single-cell RNAseq; biomarkers; for early detection;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MA12.09
引用
下载
收藏
页码:S143 / S143
页数:1
相关论文
共 45 条
  • [1] Accurate identification of single-nucleotide variants in whole-genome-amplified single cells
    Dong X.
    Zhang L.
    Milholland B.
    Lee M.
    Maslov A.Y.
    Wang T.
    Vijg J.
    Nature Methods, 2017, 14 (5) : 491 - 493
  • [2] Accurate identification of single-nucleotide variants in whole-genome-amplified single cells
    Dong, Xiao
    Zhang, Lei
    Milholland, Brandon
    Lee, Moonsook
    Maslov, Alexander Y.
    Wang, Tao
    Vijg, Jan
    NATURE METHODS, 2017, 14 (05) : 491 - +
  • [3] Identification and functional assays of single-nucleotide variants of opsins genes in melanocytic tumors
    Zhang, Wei
    Zeng, Wen
    Feng, Jianglong
    Li, Pinhao
    Wang, Yu
    Lu, Hongguang
    PIGMENT CELL & MELANOMA RESEARCH, 2022, 35 (04) : 436 - 449
  • [4] Application of RegTools to TCGA samples for the identification of tumor-specific splice variants
    Cotto, Kelsy C.
    Feng, Yang-Yang
    Skidmore, Zachary L.
    Griffith, Obi L.
    Griffith, Malachi
    CANCER RESEARCH, 2019, 79 (13)
  • [5] Identification of multiple single-nucleotide variants for clinical evaluation of Helicobacter pylori drug resistance
    Hu, Shan-Wen
    Zhang, Xiao-Rong
    Li, Wan-Xin
    Chen, Lan-Lan
    Zhao, Wei
    Xu, Jing-Juan
    Ye, Wei-Min
    TALANTA, 2022, 243
  • [6] Correction: Corrigendum: Accurate identification of single-nucleotide variants in whole-genome-amplified single cells
    Xiao Dong
    Lei Zhang
    Brandon Milholland
    Moonsook Lee
    Alexander Y Maslov
    Tao Wang
    Jan Vijg
    Nature Methods, 2017, 14 : 1222 - 1222
  • [7] Identification of Novel Single-Nucleotide Variants With Potential of Mediating Malfunction of MicroRNA in Congenital Heart Disease
    Liu, Wangkai
    Cheng, Liangping
    Chen, Ken
    Wu, Jialing
    Peng, Rui
    Tang, Yan-Lai
    Chen, Jinghai
    Yang, Yuedong
    Li, Peiqiang
    Huang, Zhan-Peng
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2021, 8
  • [8] Unbiased testing of several hundred tumor-specific single nucleotide variants of a tumor for protective immunogenicity and CD8+ response reveals surprises.
    Brennick, Cory A.
    George, Mariam M.
    Hagymasi, Adam T.
    Shcheglova, Tatiana V.
    Al Seesi, Sahar
    Mandoiu, Ion I.
    Srivastava, Pramod K.
    JOURNAL OF IMMUNOLOGY, 2018, 200 (01):
  • [9] Identification of single-nucleotide variants by high-throughput RNA sequencing in endemic Burkitt Lymphoma
    Laginestra, Maria Antonella
    Abate, Francesco
    Etebari, Maryam
    Falco, Giulia D.
    Fuligni, Fabio
    Rossi, Maura
    Zairis, Sakellarios
    Sapienza, Maria Rosaria
    Gazzola, Anna
    Mannu, Claudia
    Melle, Federica
    Agostinelli, Claudio
    Navari, Mohsen
    Bellan, Cristiana
    Gazaneo, Sara
    Mundo, Lucia
    Ogwang, Martin
    Calbi, Valeria
    Leoncini, Lorenzo
    Pileri, Stefano A.
    Rabadan, Raul
    Piccaluga, Pier Paolo
    CANCER RESEARCH, 2014, 74 (19)
  • [10] Cancer Genome Scanning in Plasma: Detection of Tumor-Associated Copy Number Aberrations, Single-Nucleotide Variants, and Tumoral Heterogeneity by Massively Parallel Sequencing
    Chan, K. C. Allen
    Jiang, Peiyong
    Zheng, Yama W. L.
    Liao, Gary J. W.
    Sun, Hao
    Wong, John
    Siu, Shing Shun N.
    Chan, Wing C.
    Chan, Stephen L.
    Chan, Anthony T. C.
    Lai, Paul B. S.
    Chiu, Rossa W. K.
    Lo, Y. M. D.
    CLINICAL CHEMISTRY, 2013, 59 (01) : 211 - 224