Correction to: Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker.

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DOI: 10.1093/bioinformatics/btag198
Published: 2026 May 3
Container: Bioinformatics (Oxford, England)
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1093/bioinformatics/btag198,
  title = {Correction to: Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker.},
  year = {2026},
  journal = {Bioinformatics (Oxford, England)},
  doi = {10.1093/bioinformatics/btag198},
  url = {https://doi.org/10.1093/bioinformatics/btag198}
}

RIS

TY  - JOUR
TI  - Correction to: Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker.
PY  - 2026
JO  - Bioinformatics (Oxford, England)
DO  - 10.1093/bioinformatics/btag198
UR  - https://doi.org/10.1093/bioinformatics/btag198
ER  -

APA

Correction to: Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker.. (2026). Bioinformatics (Oxford, England). https://doi.org/10.1093/bioinformatics/btag198

Source records

pubmed · retrieved 2026-09-25T06:15:07.946Z