Evidence map›Paper›PMID 34015059›Full record

ArticlePloS one2021

ChromInst: A single cell sequencing technique to accomplish pre-implantation comprehensive chromosomal screening overnight.

Fang-Fang Gao, Li Chen, Shi-Ping Bo, Ya-Xin Yao, Zhong-Li Xu, Qing-Yu Ding, Peng Zhang, Si-Jia Lu, Jun Ren

Abstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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  5. Review
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

9 authors.

Fang-Fang GaoDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.
Li ChenDepartment of Reproductive Medicine, Affiliated Jinling Hospital, Medicine School of Nanjing University, Nanjing, PR China.
Shi-Ping BoDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.
Ya-Xin YaoDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.
Zhong-Li XuDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.
Qing-Yu DingDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.
Peng ZhangDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.
Si-Jia LuDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.
Jun RenDepartment of Research and Development, Yikon Genomics (Suzhou) Company Limited, Suzhou, Jiangsu, PR China.ORCID 0000-0002-3351-1910

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next Generation Sequencing (NGS) is a powerful tool getting into the field of clinical examination. Its preliminary application in pre-implantation comprehensive chromosomal screening (PCCS) of assisted reproduction (test-tube baby) has shown encouraging outcomes that improves the success rate of in vitro fertilization. However, the conventional NGS library construction is time consuming. In addition with the whole genome amplification (WGA) procedure in prior, makes the single cell NGS assay hardly be accomplished within an adequately short turnover time in supporting fresh embryo implantation. In this work, we established a concise single cell sequencing protocol, ChromInst, in which the single cell WGA and NGS library construction were integrated into a two-step PCR procedure of ~ 2.5hours reaction time. We then validated the feasibility of ChromInst for overnight PCCS assay by examining 14 voluntary donated embryo biopsy samples in a single sequencing run of Miseq with merely 13M reads production. The good compatibility of ChromInst with the restriction of Illumina sequencing technique along with the good library yield uniformity resulted superior data usage efficiency and reads distribution evenness that ensures precisely distinguish of 6 normal embryos from 8 abnormal one with variable chromosomal aneuploidy. The superior succinctness and effectiveness of this protocol permits its utilization in other time limited single cell NGS applications.

Indexed as

High-Throughput Screening AssaysPreimplantation DiagnosisSingle-Cell AnalysisBiopsyBlastocystChromosomesEmbryo DispositionEmbryo ImplantationFemaleFertilization in VitroGenetic TestingGenome, HumanHigh-Throughput Nucleotide SequencingHumansPregnancyReproductive Techniques, Assisted

Identifiers

PMID34015059
PMCPMC8136696

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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.