Expanding implementation of pediatric whole-genome sequencing: Insights from SeqFirst providers to inform equitable access to a precise genetic diagnosis.

Yu JH, MacDuffie KE, Sommerland O, Theoryn T, Murali P, Anderson K, Sikes M, Kruidenier L, Gildersleeve HIS, Scott A, Buckingham KJ, McWalter K, Kruszka P, Keefe AC, Chong JX, Veenstra DL, Dipple KM, Wenger T, Doherty D, Bamshad MJ

Open source

DOI
10.1016/j.xhgg.2025.100464
Published
2025 Oct 9
Container
HGG advances
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.xhgg.2025.100464,
  title = {Expanding implementation of pediatric whole-genome sequencing: Insights from SeqFirst providers to inform equitable access to a precise genetic diagnosis.},
  author = {Yu JH and MacDuffie KE and Sommerland O and Theoryn T and Murali P and Anderson K and Sikes M and Kruidenier L and Gildersleeve HIS and Scott A and Buckingham KJ and McWalter K and Kruszka P and Keefe AC and Chong JX and Veenstra DL and Dipple KM and Wenger T and Doherty D and Bamshad MJ},
  year = {2025},
  journal = {HGG advances},
  doi = {10.1016/j.xhgg.2025.100464},
  url = {https://doi.org/10.1016/j.xhgg.2025.100464}
}

RIS

TY  - JOUR
TI  - Expanding implementation of pediatric whole-genome sequencing: Insights from SeqFirst providers to inform equitable access to a precise genetic diagnosis.
AU  - Yu JH
AU  - MacDuffie KE
AU  - Sommerland O
AU  - Theoryn T
AU  - Murali P
AU  - Anderson K
AU  - Sikes M
AU  - Kruidenier L
AU  - Gildersleeve HIS
AU  - Scott A
AU  - Buckingham KJ
AU  - McWalter K
AU  - Kruszka P
AU  - Keefe AC
AU  - Chong JX
AU  - Veenstra DL
AU  - Dipple KM
AU  - Wenger T
AU  - Doherty D
AU  - Bamshad MJ
PY  - 2025
JO  - HGG advances
DO  - 10.1016/j.xhgg.2025.100464
UR  - https://doi.org/10.1016/j.xhgg.2025.100464
ER  - 

APA

JH, Y., KE, M., O, S., T, T., P, M., K, A., M, S., L, K., HIS, G., A, S., KJ, B., K, M., P, K., AC, K., JX, C., DL, V., KM, D., T, W., D, D., & MJ, B. (2025). Expanding implementation of pediatric whole-genome sequencing: Insights from SeqFirst providers to inform equitable access to a precise genetic diagnosis.. HGG advances. https://doi.org/10.1016/j.xhgg.2025.100464

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