Long-read sequencing and benchmarking of saliva against blood for genomic variant detection in autism.

Sui Y, Campos G, Kwon Y, Wong I, Koundinya N, Munson KM, Hoekzema K, Ayllon M, Wang T, Neuhaus E, Eichler EE

DOI: 10.64898/2026.10.09.26365004
Published: 2026 Oct 13
Container: medRxiv : the preprint server for health sciences
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.64898/2026.10.09.26365004,
  title = {Long-read sequencing and benchmarking of saliva against blood for genomic variant detection in autism.},
  author = {Sui Y and Campos G and Kwon Y and Wong I and Koundinya N and Munson KM and Hoekzema K and Ayllon M and Wang T and Neuhaus E and Eichler EE},
  year = {2026},
  journal = {medRxiv : the preprint server for health sciences},
  doi = {10.64898/2026.10.09.26365004},
  url = {https://doi.org/10.64898/2026.10.09.26365004}
}

RIS

TY  - JOUR
TI  - Long-read sequencing and benchmarking of saliva against blood for genomic variant detection in autism.
AU  - Sui Y
AU  - Campos G
AU  - Kwon Y
AU  - Wong I
AU  - Koundinya N
AU  - Munson KM
AU  - Hoekzema K
AU  - Ayllon M
AU  - Wang T
AU  - Neuhaus E
AU  - Eichler EE
PY  - 2026
JO  - medRxiv : the preprint server for health sciences
DO  - 10.64898/2026.10.09.26365004
UR  - https://doi.org/10.64898/2026.10.09.26365004
ER  -

APA

Y, S., G, C., Y, K., I, W., N, K., KM, M., K, H., M, A., T, W., E, N., & EE, E. (2026). Long-read sequencing and benchmarking of saliva against blood for genomic variant detection in autism.. medRxiv : the preprint server for health sciences. https://doi.org/10.64898/2026.10.09.26365004

Source records

pubmed · retrieved 2026-11-10T11:55:54.152Z