Evidence map›Paper›PMID 38965452›Full record

ArticleClinical and translational medicine2024

Validation and depth evaluation of recurrent neural network-based ultra low-pass genome sequencing for the detection of absence of heterozygosity: A multi-centre study of 409 cases.

Yeqing Qian, Jianjun Zhu, Zhiguo Tang, Yan Sun, Zhonghua Wang, Fei Tang, Yun Yang, Linlin Fan, Yixi Sun, Bei Liu and 19 more

Abstract readLetterMulticenter StudyValidation Study
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical and translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

29 authors.

Yeqing QianDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jianjun ZhuDepartment of Fetal Medical Center, Jiaxing Maternity and Children Health Care Hospital, Jiaxing University, Jiaxing, China.
Zhiguo TangAndrological Medicine, Maternity and Child Health Hospital of Anhui Province, Affiliated Maternity and Child Health Hospital of Anhui Medical University, Hefei, China.
Yan SunBGI Genomics, Shenzhen, China.
Zhonghua WangClin Lab, BGI Genomics, Tianjin, China.
Fei TangClin Lab, BGI Genomics, Tianjin, China.
Yun YangClin Lab, BGI Genomics, Wuhan, China.
Linlin FanClin Lab, BGI Genomics, Tianjin, China.
Yixi SunDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Bei LiuDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Min ChenDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yuqin LuoDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Junjie HuDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Kai YanDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jianfen ManClin Lab, BGI Genomics, Wuhan, China.
Lina WangClin Lab, BGI Genomics, Wuhan, China.
Cangcang JiaClin Lab, BGI Genomics, Wuhan, China.
Ping TangDepartment of Fetal Medical Center, Jiaxing Maternity and Children Health Care Hospital, Jiaxing University, Jiaxing, China.
Xinyi ZhuDepartment of Fetal Medical Center, Jiaxing Maternity and Children Health Care Hospital, Jiaxing University, Jiaxing, China.
Chaohong WangMedical Genetics Center, Maternity and Child Health Hospital of Anhui Province, Affiliated Maternity and Child Health Hospital of Anhui Medical University, Hefei, China.
Junxiang TangMedical Genetics Center, Maternity and Child Health Hospital of Anhui Province, Affiliated Maternity and Child Health Hospital of Anhui Medical University, Hefei, China.
Yuanyuan XiaMedical Genetics Center, Maternity and Child Health Hospital of Anhui Province, Affiliated Maternity and Child Health Hospital of Anhui Medical University, Hefei, China.
Xueqin GuoClin Lab, BGI Genomics, Wuhan, China.
Kang ZhangClin Lab, BGI Genomics, Wuhan, China.
Xiaoli WangClin Lab, BGI Genomics, Shenzhen, China.
Suping LiDepartment of Fetal Medical Center, Jiaxing Maternity and Children Health Care Hospital, Jiaxing University, Jiaxing, China.
Lijie SongClin Lab, BGI Genomics, Tianjin, China.
Jiansheng ZhuMedical Genetics Center, Maternity and Child Health Hospital of Anhui Province, Affiliated Maternity and Child Health Hospital of Anhui Medical University, Hefei, China.
Minyue DongDepartment of Reproductive Genetics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0002-4344-7924

Funding

4+X Clinical Research Project of Women's Hospital, Zhejiang University School of Medicine ZDFY2023-4XPY201Anhui Key Research and Development Program 2022e07020031National Key R&D Program of China 2023YFC2705600Technology Bureau of Jiaxing, Zhejiang Province 2023AY31030Zhejiang Provincial Natural Science Foundation of China LY22H110004
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Loss of HeterozygosityNeural Networks, ComputerHumansWhole Genome Sequencing

Identifiers

PMID38965452
PMCPMC11223989

What OpenQuestion holds

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Registered trials

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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.