Comprehensive de novo mutation discovery with HiFi long-read sequencing
2023 · Genome Medicine · 51 citations
https://doi.org/10.1186/s13073-023-01183-6
B
Bart van der Sanden
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Bart van der Sanden is an academic researcher from Radboud University Nijmegen. The author has contributed to research in topics: Genomics and Rare Diseases & Genomics and Phylogenetic Studies & Genetic Neurodegenerative Diseases. The author has an h-index of 7, co-authored 17 publications.
ORCID: 0000-0003-0546-1351Papers by this author
worksOptical genome mapping enables accurate testing of large repeat expansions
2025 · Genome Research · 6 citations
https://doi.org/10.1101/gr.279491.124
Investigation of different ML approaches in classification of emotions induced by acute stress
2023 · Heliyon · 2 citations
https://doi.org/10.1016/j.heliyon.2023.e23611
Interrupted CTG repeats in the 37–43 units size range in the 3ʹUTR of DMPK are common alleles
2025 · European Journal of Human Genetics · 2 citations
https://doi.org/10.1038/s41431-025-01907-9
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