Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing reads.

Quinodoz M, Kaminska K, Cancellieri F, Han JH, Peter VG, Celik E, Janeschitz-Kriegl L, Schärer N, Hauenstein D, György B, Calzetti G, Hahaut V, Custódio S, Sousa AC, Wada Y, Murakami Y, Fernández AA, Hernández CR, Minguez P, Ayuso C, Nishiguchi KM, Santos C, Santos LC, Tran VH, Vaclavik V, Scholl HPN, Rivolta C

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DOI: 10.1016/j.ajhg.2024.03.001
Published: 2024 Apr 4
Container: American journal of human genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1016/j.ajhg.2024.03.001,
  title = {Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing reads.},
  author = {Quinodoz M and Kaminska K and Cancellieri F and Han JH and Peter VG and Celik E and Janeschitz-Kriegl L and Schärer N and Hauenstein D and György B and Calzetti G and Hahaut V and Custódio S and Sousa AC and Wada Y and Murakami Y and Fernández AA and Hernández CR and Minguez P and Ayuso C and Nishiguchi KM and Santos C and Santos LC and Tran VH and Vaclavik V and Scholl HPN and Rivolta C},
  year = {2024},
  journal = {American journal of human genetics},
  doi = {10.1016/j.ajhg.2024.03.001},
  url = {https://doi.org/10.1016/j.ajhg.2024.03.001}
}

RIS

TY  - JOUR
TI  - Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing reads.
AU  - Quinodoz M
AU  - Kaminska K
AU  - Cancellieri F
AU  - Han JH
AU  - Peter VG
AU  - Celik E
AU  - Janeschitz-Kriegl L
AU  - Schärer N
AU  - Hauenstein D
AU  - György B
AU  - Calzetti G
AU  - Hahaut V
AU  - Custódio S
AU  - Sousa AC
AU  - Wada Y
AU  - Murakami Y
AU  - Fernández AA
AU  - Hernández CR
AU  - Minguez P
AU  - Ayuso C
AU  - Nishiguchi KM
AU  - Santos C
AU  - Santos LC
AU  - Tran VH
AU  - Vaclavik V
AU  - Scholl HPN
AU  - Rivolta C
PY  - 2024
JO  - American journal of human genetics
DO  - 10.1016/j.ajhg.2024.03.001
UR  - https://doi.org/10.1016/j.ajhg.2024.03.001
ER  -

APA

M, Q., K, K., F, C., JH, H., VG, P., E, C., L, J., N, S., D, H., B, G., G, C., V, H., S, C., AC, S., Y, W., Y, M., AA, F., CR, H., P, M., C, A., KM, N., C, S., LC, S., VH, T., V, V., HPN, S., & C, R. (2024). Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing reads.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2024.03.001

Source records

pubmed · retrieved 2026-09-26T07:01:07.513Z