Cite
Exploring the genetic and epigenetic underpinnings of early-onset cancers: Variant prioritization for long read whole genome sequencing from family cancer pedigrees.
MLA
Kramer, Melissa, et al. “Exploring the Genetic and Epigenetic Underpinnings of Early-Onset Cancers: Variant Prioritization for Long Read Whole Genome Sequencing from Family Cancer Pedigrees.” BioRxiv : The Preprint Server for Biology, July 2024. EBSCOhost, https://doi.org/10.1101/2024.06.27.601096.
APA
Kramer, M., Goodwin, S., Wappel, R., Borio, M., Offit, K., Feldman, D. R., Stadler, Z. K., & McCombie, W. R. (2024). Exploring the genetic and epigenetic underpinnings of early-onset cancers: Variant prioritization for long read whole genome sequencing from family cancer pedigrees. BioRxiv : The Preprint Server for Biology. https://doi.org/10.1101/2024.06.27.601096
Chicago
Kramer, Melissa, Sara Goodwin, Robert Wappel, Matilde Borio, Kenneth Offit, Darren R Feldman, Zsofia K Stadler, and W Richard McCombie. 2024. “Exploring the Genetic and Epigenetic Underpinnings of Early-Onset Cancers: Variant Prioritization for Long Read Whole Genome Sequencing from Family Cancer Pedigrees.” BioRxiv : The Preprint Server for Biology, July. doi:10.1101/2024.06.27.601096.