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PreprintCC BY-NC-NDbioRxiv

OFC-SV: Interpreting structural variants in African and Asian cohorts with non-syndromic orofacial clefts

  • K. Chen
  • Y. Chung
  • T. Becker
  • D. Bayarsaihan
  • D.-G. Shin1
  1. 1University of Connecticut
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Abstract

OFC-SV is a web-based data portal designed to help interpret structural variants (SVs) in non-syndromic orofacial clefts genomic data published by The Gabriella Miller Kids First Pediatric Research Program. The portal offers a user-friendly way to explore 41 novel SV genes (of these 13 sharing regulatory perturbations already reported in the literature as SNV genes) potentially responsible for non-syndromic OFC (nsOFC) from a cohort of children of African and Asian ancestry. A salient feature of the portal is its unique ability to capture epigenomic disruptions and complex oligogenic interactions in visualized regulatory pathways, thus advancing the frontier of disease etiology through convenient translation of computational signals into biological interpretations.

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Cite

BibTeXRIS
BibTeX
@misc{chen2026ofcsv,
  title = {{OFC-SV: Interpreting structural variants in African and Asian cohorts with non-syndromic orofacial clefts}},
  author = {K. Chen and Y. Chung and T. Becker and D. Bayarsaihan and D.-G. Shin},
  howpublished = {bioRxiv},
  year = {2026},
  month = oct,
  doi = {10.64898/2026.10.13.757087},
  url = {https://www.biorxiv.org/content/10.64898/2026.10.13.757087v1},
  note = {CC BY-NC-ND},
}
RIS
TY  - UNPB
TI  - OFC-SV: Interpreting structural variants in African and Asian cohorts with non-syndromic orofacial clefts
AU  - K. Chen
AU  - Y. Chung
AU  - T. Becker
AU  - D. Bayarsaihan
AU  - D.-G. Shin
PY  - 2026
DA  - 2026/10/13
PB  - bioRxiv
DO  - 10.64898/2026.10.13.757087
UR  - https://www.biorxiv.org/content/10.64898/2026.10.13.757087v1
AB  - OFC-SV is a web-based data portal designed to help interpret structural variants (SVs) in non-syndromic orofacial clefts genomic data published by The Gabriella Miller Kids First Pediatric Research Program. The portal offers a user-friendly way to explore 41 novel SV genes (of these 13 sharing regulatory perturbations already reported in the literature as SNV genes) potentially responsible for non-syndromic OFC (nsOFC) from a cohort of children of African and Asian ancestry. A salient feature of the portal is its unique ability to capture epigenomic disruptions and complex oligogenic interactions in visualized regulatory pathways, thus advancing the frontier of disease etiology through convenient translation of computational signals into biological interpretations.
ER  -