The comparison of the performance of four whole genome amplification kits on ion proton platform in copy number variation detection

被引:14
|
作者
Zhang, Xinyi [1 ]
Liang, Bo [2 ,3 ]
Xu, Xiaoyan [1 ]
Zhou, Feifei [1 ]
Kong, Lingyin [4 ]
Shen, Jingjing [4 ]
Xia, Yingying [2 ]
Xuan, Liming [4 ]
Mao, Yan [2 ]
Xue, Yongfeng [2 ]
Liu, Caixia [5 ,6 ]
Tan, Jichun [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Gynecol & Obstet Dept, Reprod Med Ctr, Shenyang 110004, Liaoning, Peoples R China
[2] Basecare Med Device Co Ltd, Suzhou 215000, Jiangsu, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Joint Int Res Lab Metab & Dev Sci, State Key Lab Microbial Metab, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[4] Cyagen Hlth Inc, Suzhou 215400, Jiangsu, Peoples R China
[5] China Med Univ, Shengjing Hosp, Key Lab Maternal Fetal Med Liaoning Prov, Shenyang 110004, Liaoning, Peoples R China
[6] China Med Univ, Shengjing Hosp, Key Lab Obstet & Gynecol Higher Educ Liaoning Pro, Shenyang 110004, Liaoning, Peoples R China
关键词
PREIMPLANTATION GENETIC DIAGNOSIS; SINGLE-CELL; ANEUPLOIDIES;
D O I
10.1042/BSR20170252
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
With the development and clinical application of genomics, more and more concern is focused on single-cell sequencing. In the process of single-cell sequencing, whole genome amplification is a key step to enrich sample DNA. Previous studies have compared the performance of different whole genome amplification (WGA) strategies on Illumina sequencing platforms, but there is no related research aimed at Ion Proton platform, which is also a popular next-generation sequencing platform. Here by amplifying cells from six cell lines with different karyotypes, we estimated the data features of four common commercial WGA kits (PicoPLEX WGA Kit, GenomePlex Single Cell Whole Genome Amplification Kit, MALBAC Single Cell Whole Genome Amplification Kit, and REPLI-g Single Cell Kit), including median absolute pairwise difference, uniformity, reproducibility, and fidelity, and examined their performance of copy number variation detection. The results showed that both MALBAC and PicoPLEX could yield high-quality data and had high reproducibility and fidelity; and as for uniformity, PicoPLEX was slightly superior to MALBAC.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Quantitative assessment of single-cell whole genome amplification methods for detecting copy number variation using hippocampal neurons
    Luwen Ning
    Zhoufang Li
    Guan Wang
    Wen Hu
    Qingming Hou
    Yin Tong
    Meng Zhang
    Yao Chen
    Li Qin
    Xiaoping Chen
    Heng-Ye Man
    Pinghua Liu
    Jiankui He
    Scientific Reports, 5
  • [32] Detection of genome-wide copy number variation in Murrah buffaloes
    Kumar, Harshit
    Panigrahi, Manjit
    Strillacci, Maria G.
    Nayak, Sonali Sonejita
    Rajawat, Divya
    Ghildiyal, Kanika
    Bhushan, Bharat
    Dutt, Triveni
    ANIMAL BIOTECHNOLOGY, 2023, 34 (08) : 3783 - 3795
  • [33] Variability in Copy Number Variation: Detection and Comparison Across Platforms
    Doan, Betty Q.
    Scharpf, Robert
    O'Connor, Ashley
    Irizarry, Rafael
    Chakravarti, Aravinda
    GENETIC EPIDEMIOLOGY, 2009, 33 (08) : 816 - 816
  • [34] Comparison of seven single cell whole genome amplification commercial kits using targeted sequencing
    Tamir Biezuner
    Ofir Raz
    Shiran Amir
    Lilach Milo
    Rivka Adar
    Yael Fried
    Elena Ainbinder
    Ehud Shapiro
    Scientific Reports, 11
  • [35] Comparison of seven single cell whole genome amplification commercial kits using targeted sequencing
    Biezuner, Tamir
    Raz, Ofir
    Amir, Shiran
    Milo, Lilach
    Adar, Rivka
    Fried, Yael
    Ainbinder, Elena
    Shapiro, Ehud
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [36] A Survey of Copy Number Variation in the Porcine Genome Detected from Whole-Genome Sequence.
    Keel, B. N.
    Nonneman, D. J.
    Rohrer, G. A.
    JOURNAL OF ANIMAL SCIENCE, 2018, 96 : 17 - 18
  • [37] Improvement of large copy number variant detection by whole genome nanopore sequencing
    Cuenca-Guardiola, Javier
    de la Morena-Barrio, Belen
    Garcia, Juan L.
    Sanchis-Juan, Alba
    Corral, Javier
    Fernandez-Breis, Jesualdo T.
    JOURNAL OF ADVANCED RESEARCH, 2023, 50 : 145 - 158
  • [38] Whole genome analysis of DNA copy number variation using affymetrix and BAC microarrays
    Chopra, VS
    Wilson, G
    Holt, R
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 138B (01) : 99 - 99
  • [39] Whole Genome Distribution and Ethnic Differentiation of Copy Number Variation in Caucasian and Asian Populations
    Li, Jian
    Yang, Tielin
    Wang, Liang
    Yan, Han
    Zhang, Yinping
    Guo, Yan
    Pan, Feng
    Zhang, Zhixin
    Peng, Yumei
    Zhou, Qi
    He, Lina
    Zhu, Xuezhen
    Deng, Hongyi
    Levy, Shawn
    Papasian, Christopher J.
    Drees, Betty M.
    Hamilton, James J.
    Recker, Robert R.
    Cheng, Jing
    Deng, Hong-Wen
    PLOS ONE, 2009, 4 (11):
  • [40] Evaluation of copy number alternations detection tools for whole genome sequence data
    Ono, Hanako
    Gotoh, Masahiro
    Kohno, Takashi
    Shiraishi, Kouya
    CANCER SCIENCE, 2024, 115 : 1094 - 1094