Saturation-scale functional evidence supports clinical variant interpretation in Lynch syndrome.

Scott A, Hernandez F, Chamberlin A, Smith C, Karam R, Kitzman JO

Open source

DOI
10.1186/s13059-022-02839-z
Published
2022 Dec 22
Container
Genome biology
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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BibTeX

@article{allodium:10.1186/s13059-022-02839-z,
  title = {Saturation-scale functional evidence supports clinical variant interpretation in Lynch syndrome.},
  author = {Scott A and Hernandez F and Chamberlin A and Smith C and Karam R and Kitzman JO},
  year = {2022},
  journal = {Genome biology},
  doi = {10.1186/s13059-022-02839-z},
  url = {https://doi.org/10.1186/s13059-022-02839-z}
}

RIS

TY  - JOUR
TI  - Saturation-scale functional evidence supports clinical variant interpretation in Lynch syndrome.
AU  - Scott A
AU  - Hernandez F
AU  - Chamberlin A
AU  - Smith C
AU  - Karam R
AU  - Kitzman JO
PY  - 2022
JO  - Genome biology
DO  - 10.1186/s13059-022-02839-z
UR  - https://doi.org/10.1186/s13059-022-02839-z
ER  - 

APA

A, S., F, H., A, C., C, S., R, K., & JO, K. (2022). Saturation-scale functional evidence supports clinical variant interpretation in Lynch syndrome.. Genome biology. https://doi.org/10.1186/s13059-022-02839-z

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