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Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
View ORCID ProfileHannah E Roberts, Maria Lopopolo, Alistair T Pagnamenta, Eshita Sharma, Duncan Parkes, Lorne Lonie, Colin Freeman, Samantha J L Knight, Gerton Lunter, Helene Dreau, Helen Lockstone, Jenny C Taylor, Anna Schuh, Rory Bowden, David Buck
doi: https://doi.org/10.1101/2020.03.24.999870
Hannah E Roberts
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Maria Lopopolo
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Alistair T Pagnamenta
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
2National Institute for Health Research Oxford Biomedical Research Centre, Oxford, UK
Eshita Sharma
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Duncan Parkes
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Lorne Lonie
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Colin Freeman
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Samantha J L Knight
2National Institute for Health Research Oxford Biomedical Research Centre, Oxford, UK
Gerton Lunter
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
3MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK
Helene Dreau
4Oxford University Hospitals NHS Trust, Oxford, UK
5Department of Haematology, University of Oxford, Oxford, UK
Helen Lockstone
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Jenny C Taylor
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
2National Institute for Health Research Oxford Biomedical Research Centre, Oxford, UK
Anna Schuh
2National Institute for Health Research Oxford Biomedical Research Centre, Oxford, UK
4Oxford University Hospitals NHS Trust, Oxford, UK
6Department of Oncology, University of Oxford, Oxford, UK
Rory Bowden
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
David Buck
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK
Article usage
Posted March 25, 2020.
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Hannah E Roberts, Maria Lopopolo, Alistair T Pagnamenta, Eshita Sharma, Duncan Parkes, Lorne Lonie, Colin Freeman, Samantha J L Knight, Gerton Lunter, Helene Dreau, Helen Lockstone, Jenny C Taylor, Anna Schuh, Rory Bowden, David Buck
bioRxiv 2020.03.24.999870; doi: https://doi.org/10.1101/2020.03.24.999870
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Hannah E Roberts, Maria Lopopolo, Alistair T Pagnamenta, Eshita Sharma, Duncan Parkes, Lorne Lonie, Colin Freeman, Samantha J L Knight, Gerton Lunter, Helene Dreau, Helen Lockstone, Jenny C Taylor, Anna Schuh, Rory Bowden, David Buck
bioRxiv 2020.03.24.999870; doi: https://doi.org/10.1101/2020.03.24.999870
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