James Anthony Morris
James Anthony Morris
Senior Bioinformatics Analyst, CRUK Cambridge Institute
Verified email at cruk.cam.ac.uk
Cited by
Cited by
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
The UK10K project identifies rare variants in health and disease
UK10K consortium
Nature 526 (7571), 82-90, 2015
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage
I Angulo, O Vadas, F Garçon, E Banham-Hall, V Plagnol, TR Leahy, ...
Science 342 (6160), 866-871, 2013
Enhanced detection of circulating tumor DNA by fragment size analysis
F Mouliere, D Chandrananda, AM Piskorz, EK Moore, J Morris, ...
Science translational medicine 10 (466), eaat4921, 2018
Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
T Cooks, IS Pateras, LM Jenkins, KM Patel, AI Robles, J Morris, ...
Nature communications 9 (1), 1-15, 2018
optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants
TS Shah, JZ Liu, JAB Floyd, JA Morris, N Wirth, JC Barrett, CA Anderson
Bioinformatics 28 (12), 1598-1603, 2012
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
NJ Timpson, K Walter, JL Min, I Tachmazidou, G Malerba, SY Shin, ...
Nature communications 5, 4871, 2014
1000 Genomes Project Consortium A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
YOGY: a web-based, integrated database to retrieve protein orthologs and associated Gene Ontology terms
CJ Penkett, JA Morris, V Wood, J Bähler
Nucleic acids research 34 (suppl_2), W330-W334, 2006
Evoker: a visualization tool for genotype intensity data
JA Morris, JC Randall, JB Maller, JC Barrett
Bioinformatics 26 (14), 1786-1787, 2010
Association of plasma and urinary mutant DNA with clinical outcomes in muscle invasive bladder cancer
KM Patel, KE Van Der Vos, CG Smith, F Mouliere, D Tsui, J Morris, ...
Scientific reports 7 (1), 1-12, 2017
Detection of cell‐free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients
F Mouliere, R Mair, D Chandrananda, F Marass, CG Smith, J Su, J Morris, ...
EMBO molecular medicine 10 (12), 2018
Effects of collection and processing procedures on plasma circulating cell-free DNA from cancer patients
B Risberg, DWY Tsui, H Biggs, ARVM de Almagro, SJ Dawson, ...
The Journal of Molecular Diagnostics 20 (6), 883-892, 2018
Dynamics of multiple resistance mechanisms in plasma DNA during EGFR‐targeted therapies in non‐small cell lung cancer
DWY Tsui, M Murtaza, ASC Wong, OM Rueda, CG Smith, ...
EMBO molecular medicine 10 (6), 2018
Selecting short DNA fragments in plasma improves detection of circulating tumour DNA
F Mouliere, AM Piskorz, D Chandrananda, E Moore, J Morris, CG Smith, ...
BioRxiv, 134437, 2017
High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping
JE Collins, N Wali, IM Sealy, JA Morris, RJ White, SR Leonard, ...
BMC genomics 16 (1), 578, 2015
Olorin: combining gene flow with exome sequencing in large family studies of complex disease
JA Morris, JC Barrett
Bioinformatics 28 (24), 3320-3321, 2012
A Perl toolkit for LIMS development
JA Morris, SA Gayther, IJ Jacobs, C Jones
Source code for biology and medicine 3 (1), 4, 2008
A suite of Perl modules for handling microarray data
JA Morris, SA Gayther, IJ Jacobs, C Jones
Bioinformatics 24 (8), 1102-1103, 2008
CVE: an R package for interactive variant prioritisation in precision oncology
A Mock, S Murphy, J Morris, F Marass, N Rosenfeld, C Massie
BMC medical genomics 10 (1), 37, 2017
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