CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.
- DOI
- 10.1093/hmg/ddag076
- Published
- 2026 Aug 10
- Container
- Human molecular genetics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1093/hmg/ddag076,
title = {CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.},
author = {Tithi SS and Cooper-Knock J and Benatar M and Wuu J and Taylor JP and Wu G and Chen W},
year = {2026},
journal = {Human molecular genetics},
doi = {10.1093/hmg/ddag076},
url = {https://doi.org/10.1093/hmg/ddag076}
}RIS
TY - JOUR TI - CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma. AU - Tithi SS AU - Cooper-Knock J AU - Benatar M AU - Wuu J AU - Taylor JP AU - Wu G AU - Chen W PY - 2026 JO - Human molecular genetics DO - 10.1093/hmg/ddag076 UR - https://doi.org/10.1093/hmg/ddag076 ER -
APA
SS, T., J, C., M, B., J, W., JP, T., G, W., & W, C. (2026). CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.. Human molecular genetics. https://doi.org/10.1093/hmg/ddag076
Source records
- pubmed · retrieved 2026-09-24T23:54:27.151Z