Evidence map›Paper›PMID 40583136›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Genetic Deconvolution of Embryonic and Maternal Cell-Free DNA in Spent Culture Medium of Human Preimplantation Embryo Through Deep Learning.

Zhenyi Zhang, Jie Qiao, Yidong Chen, Peijie Zhou

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Observational
  5. 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

4 authors.

Zhenyi ZhangSchool of Mathematical Sciences, State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Third Hospital, Center for Machine Learning Research, Center for Quantitative Biology, Peking University, Beijing, 100871, China.ORCID https://orcid.org/0009-0009-5351-7154
Jie QiaoSchool of Mathematical Sciences, State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Third Hospital, Center for Machine Learning Research, Center for Quantitative Biology, Peking University, Beijing, 100871, China.ORCID https://orcid.org/0000-0003-2126-1376
Yidong ChenSchool of Mathematical Sciences, State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Third Hospital, Center for Machine Learning Research, Center for Quantitative Biology, Peking University, Beijing, 100871, China.
Peijie ZhouSchool of Mathematical Sciences, State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Third Hospital, Center for Machine Learning Research, Center for Quantitative Biology, Peking University, Beijing, 100871, China.ORCID https://orcid.org/0000-0002-4585-2923

Funding

Beijing Natural Science Foundation 7232203Fundamental Research Funds for the Central Universities PKU2025PKULCXQ031National Key R&D Program of China 2023YFC2705600National Key R&D Program of China 2023YFC2705602National Natural Science Foundation of China 12288101National Natural Science Foundation of China 8206100646National Natural Science Foundation of China 82301889National Natural Science Foundation of China T2321001Peking UniversityPeking University Third Hospital BYSYZD2022029
6 · The paper itself

Abstract

Noninvasive preimplantation genetic testing for aneuploidy based on embryonic cell-free DNA (cfDNA) released in spent embryo culture media (SECM) has brought hope in selecting embryos that are most likely to implant and grow into healthy babies during assisted reproduction. However, maternal DNA contamination in SECM significantly hampers the reliability of embryonic chromosome ploidy profiles, leading to false negative results, particularly at high contamination levels. Here, we present DECENT (deep copy number variation (CNV) reconstruction), a deep learning method to reconstruct embryonic CNVs and mitigate maternal contamination in SECM from single-cell methylation sequencing of cfDNA. DECENT integrates sequence features and methylation patterns by combining convolution modules, long-short memory, and attention mechanisms to infer the origin of cfDNA reads. The benchmarking study demonstrated DECENT's ability to estimate contamination proportions and restore embryonic chromosome aneuploidies in samples with varying contamination levels. In contaminated SECM clinical samples, including one with more than 80% maternal reads, DECENT achieved consistent CNV recovery with invasive tests. Overall, DECENT contributes to enhancing the diagnostic accuracy and effectiveness of cfDNA-based noninvasive preimplantation genetic testing, establishing a robust groundwork for its extensive clinical utilization in the field of reproductive medicine.

Indexed as

BlastocystCell-Free Nucleic AcidsCulture MediaDeep LearningPreimplantation DiagnosisAneuploidyDNA Copy Number VariationsDNA MethylationEmbryo Culture TechniquesFemaleHumansPregnancyCell-Free Nucleic AcidsCulture Mediadeep learningDNA methylationmaternal cumulus cell contamination removalnon‐invasive preimplantation genetic testingspent embryo culture medium

Identifiers

PMID40583136
PMCPMC12442666

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.