Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations.
- DOI
- 10.1186/s12859-017-1951-y
- Published
- 2017 Dec 1
- Container
- BMC bioinformatics
- 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.
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Cite this work
BibTeX
@article{allodium:10.1186/s12859-017-1951-y,
title = {Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations.},
author = {Broeckx BJG and Peelman L and Saunders JH and Deforce D and Clement L},
year = {2017},
journal = {BMC bioinformatics},
doi = {10.1186/s12859-017-1951-y},
url = {https://doi.org/10.1186/s12859-017-1951-y}
}RIS
TY - JOUR TI - Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations. AU - Broeckx BJG AU - Peelman L AU - Saunders JH AU - Deforce D AU - Clement L PY - 2017 JO - BMC bioinformatics DO - 10.1186/s12859-017-1951-y UR - https://doi.org/10.1186/s12859-017-1951-y ER -
APA
BJG, B., L, P., JH, S., D, D., & L, C. (2017). Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations.. BMC bioinformatics. https://doi.org/10.1186/s12859-017-1951-y
Source records
- pubmed · retrieved 2026-09-26T04:04:35.299Z