User profiles for Vincent Hanlon
Vincent CT HanlonPostdoctoral Researcher, Crop Science Centre, Cambridge University Verified email at bccrc.ca Cited by 226 |
Somatic mutations substantially increase the per-generation mutation rate in the conifer Picea sitchensis
The rates and biological significance of somatic mutations have long been a subject of debate.
Somatic mutations in plants are expected to accumulate with vegetative growth and time, …
Somatic mutations in plants are expected to accumulate with vegetative growth and time, …
[PDF][PDF] Benchmarking challenging small variants with linked and long reads
Genome in a Bottle benchmarks are widely used to help validate clinical sequencing pipelines
and develop variant calling and sequencing methods. Here we use accurate linked and …
and develop variant calling and sequencing methods. Here we use accurate linked and …
A survey of current methods to detect and genotype inversions
Polymorphic inversions are ubiquitous in humans and they have been linked to both
adaptation and disease. Following their discovery in Drosophila more than a century ago, …
adaptation and disease. Following their discovery in Drosophila more than a century ago, …
[PDF][PDF] Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq
Hundreds of loci in human genomes have alleles that are methylated differentially according
to their parent of origin. These imprinted loci generally show little variation across tissues, …
to their parent of origin. These imprinted loci generally show little variation across tissues, …
[PDF][PDF] Construction of Strand-seq libraries in open nanoliter arrays
VCT Hanlon, DD Chan, Z Hamadeh, Y Wang… - Cell reports …, 2022 - cell.com
Single-cell Strand-seq generates directional genomic information to study DNA repair, assemble
genomes, and map structural variation onto chromosome-length haplotypes. We report …
genomes, and map structural variation onto chromosome-length haplotypes. We report …
[HTML][HTML] InvertypeR: Bayesian inversion genotyping with Strand-seq data
VCT Hanlon, CA Mattsson, DCJ Spierings, V Guryev… - BMC genomics, 2021 - Springer
Background Single cell Strand-seq is a unique tool for the discovery and phasing of genomic
inversions. Conventional methods to discover inversions with Strand-seq data are blind to …
inversions. Conventional methods to discover inversions with Strand-seq data are blind to …
Chromosome-length haplotypes with StrandPhaseR and Strand-seq
VCT Hanlon, D Porubsky, PM Lansdorp - Haplotyping: Methods and …, 2022 - Springer
Dense local haplotypes can now readily be extracted from long-read or droplet-based sequence
data. However, these methods struggle to combine subchromosomal haplotype blocks …
data. However, these methods struggle to combine subchromosomal haplotype blocks …
Mapping of sister chromatid exchange events and genome alterations in single cells
Z Hamadeh, V Hanlon, PM Lansdorp - Methods, 2022 - Elsevier
Mammalian genomes encode over a hundred different helicases, many of which are implicated
in the repair of DNA lesions by acting on DNA structures arising during DNA replication, …
in the repair of DNA lesions by acting on DNA structures arising during DNA replication, …
[HTML][HTML] Days of the Hajj
V Hanlon - CMAJ, 2000 - Can Med Assoc
Canadians Out of Bounds to the man’s family. We don’t have a designated quiet room in the
emergency department for discussion of catastrophic events. A 3-way conversation ensued …
emergency department for discussion of catastrophic events. A 3-way conversation ensued …
[HTML][HTML] Körperwelten/Body Worlds
V Hanlon - CMAJ, 2003 - Can Med Assoc
Worlds Exhibition, 2003.© Prof. Dr. Gunther von Hagens, Institut für Plastination, Heidelberg,
Germany. www. bodyworlds. com into bones; the heart is a muscular pump connected to a …
Germany. www. bodyworlds. com into bones; the heart is a muscular pump connected to a …