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Puttick, C.

Publications and source records attributed to Puttick, C..

3 recordsLinked to original sources

RNA allelic frequencies of somatic mutations encode substantial functional information in cancers

A central goal of cancer research is the identification of cancer genes that drive tumour growth and progression. Existing approaches to this problem typically leverage frequentist approaches based on patterns of somatic mutagenesis in DNA. Here, we interrogate RNA variant allele frequencies to identify putative cancer genes with a novel computational tool, RVdriver, from bulk genomic-transcriptomic data within 7,948 paired exomes and transcriptomes across 30 cancer types. An elevated RNA VAF reflects a signal from multiple biological features: clonal mutations; mutations retained or gained during somatic copy-number alterations; mutations favoured by allele-specific expression; and mutations in genes expressed preferentially by the tumour compartment of admixed bulk samples. RVdriver, a statistical approach that classifies RNA VAFs of nonsynonymous mutations relative to a synonymous mutation background, leverages this information to identify known, as well as putatively novel, cancer genes, with comparable performance to DNA-based approaches. Furthermore, we demonstrate RNA VAFs of individual mutations are able to distinguish driver from passenger mutations within established cancer genes. Low-RNA VAF EGFR mutations otherwise annotated as drivers of glioblastoma by DNA tools harbour a phenotype of reduced EGFR signalling, whilst high-RNA VAF KDM6A mutations otherwise annotated as passengers exhibit a driver-like H3K27me3 expression profile, demonstrating the value of our approach in phenotyping tumours. Overall, our study showcases a novel approach for cancer gene discovery, and highlights the potential value of multi-omic and systems-biology approaches in finding novel therapeutic vulnerabilities in cancer to bring about patient benefit.

cancer biology↗

mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data

MotivationMitochondrial diseases (MDs) are the most common group of inherited metabolic disorders and are often challenging to diagnose due to extensive genotype-phenotype heterogeneity. MDs are caused by mutations in the nuclear or mitochondrial genome, where pathogenic mitochondrial variants are usually heteroplasmic and typically at much lower allelic fraction in the blood than affected tissues. Both genomes can now be readily analysed using unbiased whole genome sequencing (WGS), but most nuclear variant detection methods fail to detect low heteroplasmy variants in the mitochondrial genome. ResultsWe present mity, a bioinformatics pipeline for detecting and interpreting heteroplasmic SNVs and INDELs in the mitochondrial genome using WGS data. In 2,980 healthy controls, we observed on average 3,166x coverage in the mitochondrial genome using WGS from blood. mity utilises this high depth to detect pathogenic mitochondrial variants, even at low heteroplasmy. mity enables easy interpretation of mitochondrial variants and can be incorporated into existing diagnostic WGS pipelines. This could simplify the diagnostic pathway, avoid invasive tissue biopsies and increase the diagnostic rate for MDs and other conditions caused by impaired mitochondrial function. Availabilitymity is available from https://github.com/KCCG/mityunder an MIT license. Contactclare.puttick@crick.ac.uk, carolyn.sue@sydney.edu.au, MCowley@ccia.org.au

bioinformatics↗

The Medical Genome Reference Bank: Whole genomes and phenotype of 2,570 healthy elderly

Population health research is increasingly focused on the genetic determinants of healthy ageing, but there is no public resource of whole genome sequences and phenotype data from healthy elderly individuals. Here we describe the Medical Genome Reference Bank (MGRB), comprising whole genome sequence and phenotype of 2,570 elderly Australians depleted for cancer, cardiovascular disease, and dementia. We analysed the MGRB for single-nucleotide, indel and structural variation in the nuclear and mitochondrial genomes. Individuals in the MGRB had fewer disease-associated common and rare germline variants, relative to both cancer cases and the gnomAD and UK BioBank cohorts, consistent with risk depletion. Pervasive age-related somatic changes were correlated with grip strength in men, suggesting blood-derived whole genomes may also provide a biologic measure of age-related functional deterioration. The MGRB provides a broadly applicable reference cohort for clinical genetics and genomic association studies, and for understanding the genetics of healthy ageing. This research has been conducted using the UK Biobank Resource under Application Number 17984.

genomics↗