Whole genome amplification on single cell

被引:2
|
作者
D'Argenio, Valeria
Tomaiuolo, Rossella
Cariati, Federica [1 ]
机构
[1] CEINGE Biotecnol Avanzate Scarl, Via G Salvatore 486, I-80131 Naples, Italy
关键词
D O I
10.19186/BC_2016.034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The whole genome amplification (WGA) is a method for an entire genome amplification, starting with low amounts of DNA. Particularly, it allows downstream analysis, such as genomic screening [i.e., comparative genomic hybridization (CGH) array, next generation sequencing] and single gene mutation detection in single cells. Because WGA could introduce few bias, dependent on different methods, their selection should be related to the application. The first WGA method was based on amplification reaction and differently from a regular polymerase chain reaction (PCR), in which a single genetic locus is amplified, different locus were amplified simultaneously. Nowadays, several methods have been developed for WGA: degenerate oligonucleotide PCR and primer extension preamplification based on PCR, and multiple displacement amplification achieved with isothermal reaction setup. Each WGA approach has limitations, such as the genome coverage, chimeric DNA molecules, preferential allele amplification or allele drop-out and the guanine-cytosine (GC) richness (GC%). In this review, we detailed different WGA methods for single cell and their most important applications, such as cancer diagnosis and reproductive medicine.
引用
收藏
页码:293 / 301
页数:9
相关论文
共 50 条
  • [31] Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays
    Treff, Nathan R.
    Su, Jing
    Tao, Xin
    Levy, Brynn
    Scott, Richard T.
    FERTILITY AND STERILITY, 2010, 94 (06) : 2017 - 2021
  • [32] Manipulation of a Single Circulating Tumor Cell Using Visualization of Hydrogel Encapsulation toward Single-Cell Whole-Genome Amplification
    Yoshino, Tomoko
    Tanaka, Tsuyoshi
    Nakamura, Seita
    Negishi, Ryo
    Hosokawa, Masahito
    Matsunaga, Tadashi
    ANALYTICAL CHEMISTRY, 2016, 88 (14) : 7230 - 7237
  • [33] Single-cell isolation from cell suspensions and whole genome amplification from single cells to provide templates for CGH analysis
    Jochen B Geigl
    Michael R Speicher
    Nature Protocols, 2007, 2 : 3173 - 3184
  • [34] Single-cell isolation from cell suspensions and whole genome amplification from single cells to provide templates for CGH analysis
    Geigl, Jochen B.
    Speicher, Michael R.
    NATURE PROTOCOLS, 2007, 2 (12) : 3173 - 3184
  • [35] Single-cell whole-genome analyses by Linear Amplification via Transposon Insertion (LIANTI)
    Chen, Chongyi
    Xing, Dong
    Tan, Longzhi
    Li, Heng
    Zhou, Guangyu
    Huang, Lei
    Xie, X. Sunney
    SCIENCE, 2017, 356 (6334) : 189 - 194
  • [36] Single-Circulating Tumor Cell Whole Genome Amplification to Unravel Cancer Heterogeneity and Actionable Biomarkers
    Khan, Tanzila
    Becker, Therese M.
    Po, Joseph W.
    Chua, Wei
    Ma, Yafeng
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (15)
  • [37] PREIMPLANTATION SINGLE-CELL ANALYSIS OF MULTIPLE GENETIC-LOCI BY WHOLE-GENOME AMPLIFICATION
    SNABES, MC
    CHONG, SS
    SUBRAMANIAN, SB
    KRISTJANSSON, K
    DISEPIO, D
    HUGHES, MR
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (13) : 6181 - 6185
  • [38] Whole-genome multiple displacement amplification from single cells
    Spits, Claudia
    Le Caignec, Cedric
    De Rycke, Martine
    Van Haute, Lindsey
    Van Steirteghem, Andre
    Liebaers, Inge
    Sermon, Karen
    NATURE PROTOCOLS, 2006, 1 (04) : 1965 - 1970
  • [39] Whole-genome multiple displacement amplification from single cells
    Claudia Spits
    Cédric Le Caignec
    Martine De Rycke
    Lindsey Van Haute
    André Van Steirteghem
    Inge Liebaers
    Karen Sermon
    Nature Protocols, 2006, 1 : 1965 - 1970
  • [40] Genetic analyses of single rust spores facilitated by whole genome amplification
    Orquera, G.
    Garzon, C.
    Marek, S.
    PHYTOPATHOLOGY, 2014, 104 (05) : 8 - 8