NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling.

Hanssen F, Gabernet G, Bäuerle F, Stöcker B, Wiegand F, Smith NH, Mertes C, Neogi AG, Brandhoff L, Ossowski A, Altmueller J, Becker K, Petzold A, Sturm M, Stöcker T, Sivalingam S, Brand F, Schmidt A, Buness A, Probst AJ, Motameny S, Köster J

Open source

DOI: 10.12688/f1000research.140344.2
Published: 2023
Container: F1000Research
Publisher: Not recorded
Open access: yes

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

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Cite this work

BibTeX

@article{allodium:10.12688/f1000research.140344.2,
  title = {NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling.},
  author = {Hanssen F and Gabernet G and Bäuerle F and Stöcker B and Wiegand F and Smith NH and Mertes C and Neogi AG and Brandhoff L and Ossowski A and Altmueller J and Becker K and Petzold A and Sturm M and Stöcker T and Sivalingam S and Brand F and Schmidt A and Buness A and Probst AJ and Motameny S and Köster J},
  year = {2023},
  journal = {F1000Research},
  doi = {10.12688/f1000research.140344.2},
  url = {https://doi.org/10.12688/f1000research.140344.2}
}

RIS

TY  - JOUR
TI  - NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling.
AU  - Hanssen F
AU  - Gabernet G
AU  - Bäuerle F
AU  - Stöcker B
AU  - Wiegand F
AU  - Smith NH
AU  - Mertes C
AU  - Neogi AG
AU  - Brandhoff L
AU  - Ossowski A
AU  - Altmueller J
AU  - Becker K
AU  - Petzold A
AU  - Sturm M
AU  - Stöcker T
AU  - Sivalingam S
AU  - Brand F
AU  - Schmidt A
AU  - Buness A
AU  - Probst AJ
AU  - Motameny S
AU  - Köster J
PY  - 2023
JO  - F1000Research
DO  - 10.12688/f1000research.140344.2
UR  - https://doi.org/10.12688/f1000research.140344.2
ER  -

APA

F, H., G, G., F, B., B, S., F, W., NH, S., C, M., AG, N., L, B., A, O., J, A., K, B., A, P., M, S., T, S., S, S., F, B., A, S., A, B., AJ, P., S, M., & J, K. (2023). NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling.. F1000Research. https://doi.org/10.12688/f1000research.140344.2

Source records

pubmed · retrieved 2026-09-25T17:02:35.637Z