Published in
American Association for the Advancement of Science, Science Translational Medicine, 548(12), 2020
DOI: 10.1126/scitranslmed.aaz8084
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ctDNA monitoring using patient-specific sequencing and integration of variant reads
Journal article published in 2020 by
Jonathan C. M. Wan 
,
Katrin Heider ,
Davina Gale ,
Suzanne Murphy,
Eyal Fisher ,
Florent Mouliere ,
Andrea Ruiz-Valdepenas,
Angela Santonja ,
James Morris,
Dineika Chandrananda ,
Andrea Marshall ,
Andrew B. Gill ,
Pui Ying Chan ,
Emily Barker ,
Gemma Young
and other authors.
,
Katrin Heider ,
Davina Gale ,
Suzanne Murphy,
Eyal Fisher ,
Florent Mouliere ,
Andrea Ruiz-Valdepenas,
Angela Santonja ,
James Morris,
Dineika Chandrananda ,
Andrea Marshall ,
Andrew B. Gill ,
Pui Ying Chan ,
Emily Barker ,
Gemma Young
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
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Abstract
Integration of variant reads across patient-specific mutation loci enables sensitive ctDNA quantification in plasma cell-free DNA sequencing data.