Evidence map›Paper›PMID 36450740›Full record

ArticleNature communications2022

Automated high-throughput genome editing platform with an AI learning in situ prediction model.

Siwei Li, Jingjing An, Yaqiu Li, Xiagu Zhu, Dongdong Zhao, Lixian Wang, Yonghui Sun, Yuanzhao Yang, Changhao Bi, Xueli Zhang and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
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  8. Article
  9. Review
  10. Artificial intelligence in medical science: a review.Irish journal of medical science · 2024
    Review
  11. Promising non-model microbial cell factories obtained by genome reduction.Frontiers in bioengineering and biotechnology · 2024
    Review
  12. Review
  13. 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

11 authors.

Siwei Li *Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.ORCID 0000-0001-6057-2957
Jingjing An *Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Yaqiu Li *Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Xiagu ZhuTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Dongdong ZhaoTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.ORCID 0000-0001-9691-1308
Lixian WangTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Yonghui SunTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Yuanzhao YangTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Changhao BiTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China. bi_ch@tib.cas.cn.ORCID 0000-0002-1940-8511
Xueli ZhangTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China. zhang_xl@tib.cas.cn.ORCID 0000-0002-8660-4037
Meng WangTianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China. wangmeng@tib.cas.cn.ORCID 0000-0001-7648-9955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A great number of cell disease models with pathogenic SNVs are needed for the development of genome editing based therapeutics or broadly basic scientific research. However, the generation of traditional cell disease models is heavily dependent on large-scale manual operations, which is not only time-consuming, but also costly and error-prone. In this study, we devise an automated high-throughput platform, through which thousands of samples are automatically edited within a week, providing edited cells with high efficiency. Based on the large in situ genome editing data obtained by the automatic high-throughput platform, we develop a Chromatin Accessibility Enabled Learning Model (CAELM) to predict the performance of cytosine base editors (CBEs), both chromatin accessibility and the context-sequence are utilized to build the model, which accurately predicts the result of in situ base editing. This work is expected to accelerate the development of BE-based genetic therapies.

Indexed as

Gene EditingNamesArtificial IntelligenceChromatinLearningChromatin

Identifiers

PMID36450740
PMCPMC9712529

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.