| Benchmarking challenging small variants with linked and long reads J Wagner, ND Olson, L Harris, Z Khan, J Farek, M Mahmoud, A Stankovic, ... Cell genomics 2 (5), 2022 | 153 | 2022 |
| Somatic mutations substantially increase the per-generation mutation rate in the conifer Picea sitchensis VCT Hanlon, SP Otto, SN Aitken Evolution letters 3 (4), 348-358, 2019 | 68* | 2019 |
| Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq V Akbari*, VCT Hanlon*, K O’Neill, L Lefebvre, KA Schrader, ... Cell Genomics 3 (1), 100233, 2023 | 27 | 2023 |
| Construction of Strand-seq libraries in open nanoliter arrays VCT Hanlon, DD Chan, Z Hamadeh, Y Wang, CA Mattsson, ... Cell reports methods 2 (1), 2022 | 23 | 2022 |
| A survey of current methods to detect and genotype inversions VCT Hanlon, PM Lansdorp, V Guryev Human Mutation 43 (11), 1576-1589, 2022 | 21 | 2022 |
| A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigree D Porubsky, H Dashnow, TA Sasani, GA Logsdon, P Hallast, MD Noyes, ... bioRxiv, 2024 | 15 | 2024 |
| Mapping of sister chromatid exchange events and genome alterations in single cells Z Hamadeh, V Hanlon, PM Lansdorp Methods 204, 64-72, 2022 | 7 | 2022 |
| Chromosome-length haplotypes with StrandPhaseR and Strand-seq VCT Hanlon*, D Porubsky*, PM Lansdorp, (* denotes equal contributions) Haplotyping, 183-200, 2023 | 6 | 2023 |
| InvertypeR: Bayesian inversion genotyping with Strand-seq data VCT Hanlon, CA Mattsson, DCJ Spierings, V Guryev*, PM Lansdorp*, ... BMC genomics 22 (1), 1-8, 2021 | 6 | 2021 |
| Heritable somatic mutations accumulate slowly in Sitka spruce but increase the per-generation mutation rate considerably VCT Hanlon MSc Dissertation, University of British Columbia, 2018 | 3 | 2018 |
| Accurate parent-of-origin variant assignment for multiple hereditary cancer syndromes using proband-only blood sample analysis. KA Schrader, V Akbari, V Hanlon, T Leung, K Dixon, K O'Neill, A Roston, ... Journal of Clinical Oncology 42 (16_suppl), 10516-10516, 2024 | | 2024 |
| Method and apparatus for parent-of-origin disease allele detection for the diagnosis and management of genetic diseases P Lansdorp, K Schrader, S Jones, V Hanlon, V Akbari, K O'neill US Patent App. 18/518,079, 2024 | | 2024 |
| P658: Detection of variant parent-of-origin in diverse hereditary cancer syndromes using only the proband’s blood sample K Schrader, V Akbari, V Hanlon, T Leung, K Dixon, K O’Neill, A Roston, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| Accurate inference of parent-of-origin of pathogenic variants in SDHD without parental data K Schrader, V Akbari, V Hanlon, K Dixon, K O'Neill, Y Shen, A Sharma, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 626-626, 2024 | | 2024 |
| O35: Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants in SDHD without parental data K Schrader, V Akbari, V Hanlon, K Dixon, K O’Neill, Y Shen, A Sharma, ... Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| Smaller, denser, smarter: Improved Strand-seq library preparation, inversion genotyping, and phasing VCT Hanlon University of Groningen, 2023 | | 2023 |
Peter LansdorpBC Cancer Agencyכתובת אימייל מאומתת בדומיין bccrc.ca
