Identification of breakpoint regions and single nucleotide variations of RHD hybrid alleles by long-read sequencing.

Chang TC, Yu J, Ju B, Kim T, Loyd M, Ridout G, Neale G, Hankins JS, Weiss MJ, Ochoa G, Vege S, Chou ST, Easton J, Zheng Y

Open source

DOI
10.1111/vox.70292
Published
2026 Aug
Container
Vox sanguinis
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.

Show all credibility signals

Cite this work

BibTeX

@article{allodium:10.1111/vox.70292,
  title = {Identification of breakpoint regions and single nucleotide variations of RHD hybrid alleles by long-read sequencing.},
  author = {Chang TC and Yu J and Ju B and Kim T and Loyd M and Ridout G and Neale G and Hankins JS and Weiss MJ and Ochoa G and Vege S and Chou ST and Easton J and Zheng Y},
  year = {2026},
  journal = {Vox sanguinis},
  doi = {10.1111/vox.70292},
  url = {https://doi.org/10.1111/vox.70292}
}

RIS

TY  - JOUR
TI  - Identification of breakpoint regions and single nucleotide variations of RHD hybrid alleles by long-read sequencing.
AU  - Chang TC
AU  - Yu J
AU  - Ju B
AU  - Kim T
AU  - Loyd M
AU  - Ridout G
AU  - Neale G
AU  - Hankins JS
AU  - Weiss MJ
AU  - Ochoa G
AU  - Vege S
AU  - Chou ST
AU  - Easton J
AU  - Zheng Y
PY  - 2026
JO  - Vox sanguinis
DO  - 10.1111/vox.70292
UR  - https://doi.org/10.1111/vox.70292
ER  - 

APA

TC, C., J, Y., B, J., T, K., M, L., G, R., G, N., JS, H., MJ, W., G, O., S, V., ST, C., J, E., & Y, Z. (2026). Identification of breakpoint regions and single nucleotide variations of RHD hybrid alleles by long-read sequencing.. Vox sanguinis. https://doi.org/10.1111/vox.70292

Source records