User profiles for D. Waggott
Daryl WaggottGenome Canada Verified email at genomecanada.ca Cited by 10376 |
Genomic hallmarks of localized, non-indolent prostate cancer
…, JF Hopkins, SK Govind, C Fung, D Waggott… - Nature, 2017 - nature.com
Prostate tumours are highly variable in their response to therapies, but clinically available
prognostic factors can explain only a fraction of this heterogeneity. Here we analysed 200 …
prognostic factors can explain only a fraction of this heterogeneity. Here we analysed 200 …
Spatial genomic heterogeneity within localized, multifocal prostate cancer
Herein we provide a detailed molecular analysis of the spatial heterogeneity of clinically
localized, multifocal prostate cancer to delineate new oncogenes or tumor suppressors. We …
localized, multifocal prostate cancer to delineate new oncogenes or tumor suppressors. We …
[HTML][HTML] Accuracy in wrist-worn, sensor-based measurements of heart rate and energy expenditure in a diverse cohort
The ability to measure physical activity through wrist-worn devices provides an opportunity for
cardiovascular medicine. However, the accuracy of commercial devices is largely unknown…
cardiovascular medicine. However, the accuracy of commercial devices is largely unknown…
Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes
OBJECTIVE Despite extensive evidence for genetic susceptibility to diabetic nephropathy,
the identification of susceptibility genes and their variants has had limited success. To search …
the identification of susceptibility genes and their variants has had limited success. To search …
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
The QT interval, an electrocardiographic measure reflecting myocardial repolarization, is a
heritable trait. QT prolongation is a risk factor for ventricular arrhythmias and sudden cardiac …
heritable trait. QT prolongation is a risk factor for ventricular arrhythmias and sudden cardiac …
[HTML][HTML] Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection
The detection of somatic mutations from cancer genome sequences is key to understanding
the genetic basis of disease progression, patient survival and response to therapy. …
the genetic basis of disease progression, patient survival and response to therapy. …
[HTML][HTML] New susceptibility loci associated with kidney disease in type 1 diabetes
Diabetic kidney disease, or diabetic nephropathy (DN), is a major complication of diabetes
and the leading cause of end-stage renal disease (ESRD) that requires dialysis treatment or …
and the leading cause of end-stage renal disease (ESRD) that requires dialysis treatment or …
[HTML][HTML] Long-read genome sequencing identifies causal structural variation in a Mendelian disease
Purpose Current clinical genomics assays primarily utilize short-read sequencing (SRS),
but SRS has limited ability to evaluate repetitive regions and structural variants. Long-read …
but SRS has limited ability to evaluate repetitive regions and structural variants. Long-read …
NanoStringNorm: an extensible R package for the pre-processing of NanoString mRNA and miRNA data
Motivation: The NanoString nCounter Platform is a new and promising technology for
measuring nucleic acid abundances. It has several advantages over PCR-based techniques, …
measuring nucleic acid abundances. It has several advantages over PCR-based techniques, …
Hotspot activating PRKD1 somatic mutations in polymorphous low-grade adenocarcinomas of the salivary glands
I Weinreb, S Piscuoglio, LG Martelotto, D Waggott… - Nature …, 2014 - nature.com
Polymorphous low-grade adenocarcinoma (PLGA) is the second most frequent type of malignant
tumor of the minor salivary glands. We identified PRKD1 hotspot mutations encoding p.…
tumor of the minor salivary glands. We identified PRKD1 hotspot mutations encoding p.…