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Scientific Reports|August 1, 2024
Complete de novo assembly of Wolbachia endosymbiont of Drosophila willistoni using long-read genome sequencingJodie Jacobs, Anne Nakamoto, Mira Mastoras, et al.Research Square|July 1, 2024
Complete de novo assembly of Wolbachia endosymbiont of Drosophila willistoni using long-read genome sequencingJodie Jacobs, Anne Nakamoto, Mira Mastoras, et al.Biorxiv : the Preprint Server for Biology|March 18, 2026
Evaluating genome assemblies with HMM-FlaggerMobin Asri, Jordan M Eizenga, Prajna Hebbar, et al.American Journal of Medical Genetics. Part A|June 25, 2022
De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndromeMonica Penon-Portmann, Mohammad K Eldomery, Lorraine Potocki, et al.Biorxiv : the Preprint Server for Biology|February 27, 2026
Fully T2T pedigree assemblies reveal genetic stability and epigenetic plasticity of human centromeres across inheritance and cell-fate transitionsShihua Dong, Xiaoyun Xing, Monika Cechova, et al.Microbiology Resource Announcements|April 30, 2026
Complete de novo assembly of Wolbachia endosymbiont of contemporary Drosophila simulans using long-read genome sequencingJodie Jacobs, Alexandra Lum, Elyse Mina, et al.Journal of Medical Genetics|February 14, 2023
Recurrent, founder and hypomorphic variants contribute to the genetic landscape of Joubert syndromeValentina Serpieri, Giulia Mortarini, Hailey Loucks, et al.Biorxiv : the Preprint Server for Biology|April 10, 2026
Haplotype-resolved centromeric chromatin organization from a complete diploid human genomeYuan Xu, Hailey Loucks, Julian Menendez, et al.Journal of Medical Genetics|October 22, 2021
SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrumValentina Serpieri, Fulvio D'Abrusco, Jennifer C Dempsey, et al.Biorxiv : the Preprint Server for Biology|April 3, 2026
A Complete Genome for the Common MarmosetPrajna Hebbar, Tamara Potapova, Hailey Loucks, et al.Pageof 2