Systematic evaluation of whole exome sequencing for copy number variation detection in prenatal diagnosis.

Yu L, Hu R, Wang X, Liu Y, Tan H, Dou H, Kong Y, Lu J, Ding H, Zeng Y, Yao C, Pan L, Chen S, Zhang Y, Yin A

DOI: 10.1002/ctm2.70761
Published: 2026 Sep
Container: Clinical and translational medicine
Publisher: Not recorded
Open access: yes

Credibility signals

limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

cautionDOI registered: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
cautionDOI resolves: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility. Source: DOAJ; license: CC0
not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredROR affiliation: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
not scoredPublication license: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.1002/ctm2.70761,
  title = {Systematic evaluation of whole exome sequencing for copy number variation detection in prenatal diagnosis.},
  author = {Yu L and Hu R and Wang X and Liu Y and Tan H and Dou H and Kong Y and Lu J and Ding H and Zeng Y and Yao C and Pan L and Chen S and Zhang Y and Yin A},
  year = {2026},
  journal = {Clinical and translational medicine},
  doi = {10.1002/ctm2.70761},
  url = {https://doi.org/10.1002/ctm2.70761}
}

RIS

TY  - JOUR
TI  - Systematic evaluation of whole exome sequencing for copy number variation detection in prenatal diagnosis.
AU  - Yu L
AU  - Hu R
AU  - Wang X
AU  - Liu Y
AU  - Tan H
AU  - Dou H
AU  - Kong Y
AU  - Lu J
AU  - Ding H
AU  - Zeng Y
AU  - Yao C
AU  - Pan L
AU  - Chen S
AU  - Zhang Y
AU  - Yin A
PY  - 2026
JO  - Clinical and translational medicine
DO  - 10.1002/ctm2.70761
UR  - https://doi.org/10.1002/ctm2.70761
ER  -

APA

L, Y., R, H., X, W., Y, L., H, T., H, D., Y, K., J, L., H, D., Y, Z., C, Y., L, P., S, C., Y, Z., & A, Y. (2026). Systematic evaluation of whole exome sequencing for copy number variation detection in prenatal diagnosis.. Clinical and translational medicine. https://doi.org/10.1002/ctm2.70761

Source records

pubmed · retrieved 2026-09-25T08:57:47.263Z