Research Topics
| John C MarioniSummaryAffiliation: University of Cambridge Country: UK Publications
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Detail Information
Publications
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridizationJohn C Marioni
Computational Biology Group, Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Centre for Mathematical Sciences, Wilberforce Road, Cambridge CB3 0WA, UK
Genome Biol 8:R228. 2007..However, methods for analyzing the complex data produced and identifying regions of CNV are still being refined...
RNA-seq: an assessment of technical reproducibility and comparison with gene expression arraysJohn C Marioni
Department of Human Genetics, University of Chicago, Chicago, Illinois 60637, USA
Genome Res 18:1509-17. 2008..Based on our observations, we propose an empirical protocol and a statistical framework for the analysis of gene expression using ultra-high-throughput sequencing technology...
BioHMM: a heterogeneous hidden Markov model for segmenting array CGH dataJ C Marioni
Hutchison MRC Research Centre, Department of Oncology, Computational Biology Group, University of Cambridge Hills Road, Cambridge
Bioinformatics 22:1144-6. 2006..By utilizing a heterogeneous hidden Markov model, BioHMM incorporates relevant biological factors (e.g. the distance between adjacent clones) in the segmentation process...
Hidden copy number variation in the HapMap populationJohn C Marioni
Department of Oncology, Computational Biology Group, University of Cambridge, Cancer Research UK Cambridge Research Institute, Robinson Way, Cambridge, United Kingdom
Proc Natl Acad Sci U S A 105:10067-72. 2008..Finally, we discuss how this methodology might be applied to future studies to obtain better estimates of the extent of CNV across the genome...
High-resolution aCGH and expression profiling identifies a novel genomic subtype of ER negative breast cancerSuet F Chin
Breast Cancer Functional Genomics, Cancer Research UK Cambridge Research Institute and Department of Oncology University of Cambridge, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK
Genome Biol 8:R215. 2007..To date, most genome-wide array comparative genomic hybridization studies have used tumor panels of relatively large tumor size and high Nottingham Prognostic Index (NPI) that are not as representative of breast cancer demographics...
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysisThomas A Down
Wellcome Trust Cancer Research UK Gurdon Institute, and Department of Genetics, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK
Nat Biotechnol 26:779-85. 2008....
The pitfalls of platform comparison: DNA copy number array technologies assessedChristina Curtis
Department of Oncology, University of Cambridge, Addenbrooke s Hopsital, Hills Road, Cambridge CB20XZ, UK
BMC Genomics 10:588. 2009..By careful consideration and avoidance of potential sources of bias, we aim to provide a fair assessment of platform performance...
ESR1 gene amplification in breast cancer: a common phenomenon?Lindsay A Brown
Nat Genet 40:806-7; author reply 810-2. 2008
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs)Vardhman K Rakyan
Institute of Cell and Molecular Science, Barts and The London, London E1 2AT, United Kingdom
Genome Res 18:1518-29. 2008....
Numbers of copy-number variations and false-negative rates will be underestimated if we do not account for the dependence between repeated experimentsAndy G Lynch
Am J Hum Genet 81:418-20; author reply 420-1. 2007
