Evidence map›Paper›PMID 28572171›Full record

ArticleBioscience reports2017

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

Xinyi Zhang, Bo Liang, Xiaoyan Xu, Feifei Zhou, Lingyin Kong, Jingjing Shen, Yingying Xia, Liming Xuan, Yan Mao, Yongfeng Xue and 2 more

Abstract read
In one paragraph

Article in Bioscience reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Chromosome instability and aneuploidy in the mammalian brain.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Xinyi ZhangReproductive Medical Center of Gynecology and Obstetrics Department, Shengjing Hospital Affiliated to China Medical University, Shenyang, Liaoning 110004, China.
Bo LiangBasecare Medical Device Co., Ltd., Suzhou, Jiangsu 215000, China.
Xiaoyan XuReproductive Medical Center of Gynecology and Obstetrics Department, Shengjing Hospital Affiliated to China Medical University, Shenyang, Liaoning 110004, China.
Feifei ZhouReproductive Medical Center of Gynecology and Obstetrics Department, Shengjing Hospital Affiliated to China Medical University, Shenyang, Liaoning 110004, China.
Lingyin KongCyagen Health Inc., Suzhou, Jiangsu 215400, China.
Jingjing ShenCyagen Health Inc., Suzhou, Jiangsu 215400, China.
Yingying XiaBasecare Medical Device Co., Ltd., Suzhou, Jiangsu 215000, China.
Liming XuanCyagen Health Inc., Suzhou, Jiangsu 215400, China.
Yan MaoBasecare Medical Device Co., Ltd., Suzhou, Jiangsu 215000, China.
Yongfeng XueBasecare Medical Device Co., Ltd., Suzhou, Jiangsu 215000, China.
Caixia LiuKey Laboratory of Maternal-Fetal Medicine of Liaoning Province, Shengjing Hospital Affiliated to China Medical University, Shenyang, Liaoning 110004, China.
Jichun TanReproductive Medical Center of Gynecology and Obstetrics Department, Shengjing Hospital Affiliated to China Medical University, Shenyang, Liaoning 110004, China tjczjh@163.com liucx1716@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

DNA Copy Number VariationsGenome, HumanReagent Kits, DiagnosticCell LineHumansNucleic Acid Amplification TechniquesReagent Kits, DiagnosticCNVIon Protonsingle-cell sequencingWGA

Identifiers

PMID28572171
PMCPMC6434089

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.