TY - JOUR
T1 - Single Molecule Fluorescence Microscopy and Machine Learning for Rhesus D Antigen Classification
AU - Borgmann, Daniela Martina
AU - Mayr, Sandra
AU - Polin, Helene
AU - Schaller, Susanne
AU - Dorfer, Viktoria
AU - Obritzberger, Lisa
AU - Endmayr, Tanja
AU - Gabriel, Christian
AU - Winkler, Stephan
AU - Jacak, Jaroslaw
PY - 2016/9/1
Y1 - 2016/9/1
N2 - In transfusion medicine, the identification of the Rhesus D type is important to prevent anti-D immunisation in Rhesus D negative recipients. In particular, the detection of the very low expressed DEL phenotype is crucial and hence constitutes the bottleneck of standard immunohaematology. The current method of choice, adsorption-elution, does not provide unambiguous results. We have developed a complementary method of high sensitivity that allows reliable identification of D antigen expression. Here, we present a workflow composed of high-resolution fluorescence microscopy, image processing, and machine learning that - for the first time - enables the identification of even small amounts of D antigen on the cellular level. The high sensitivity of our technique captures the full range of D antigen expression (including D+, weak D, DEL, D−), allows automated population analyses, and results in classification test accuracies of up to 96%, even for very low expressed phenotypes.
AB - In transfusion medicine, the identification of the Rhesus D type is important to prevent anti-D immunisation in Rhesus D negative recipients. In particular, the detection of the very low expressed DEL phenotype is crucial and hence constitutes the bottleneck of standard immunohaematology. The current method of choice, adsorption-elution, does not provide unambiguous results. We have developed a complementary method of high sensitivity that allows reliable identification of D antigen expression. Here, we present a workflow composed of high-resolution fluorescence microscopy, image processing, and machine learning that - for the first time - enables the identification of even small amounts of D antigen on the cellular level. The high sensitivity of our technique captures the full range of D antigen expression (including D+, weak D, DEL, D−), allows automated population analyses, and results in classification test accuracies of up to 96%, even for very low expressed phenotypes.
UR - http://www.scopus.com/inward/record.url?scp=84984914444&partnerID=8YFLogxK
U2 - 10.1038/srep32317
DO - 10.1038/srep32317
M3 - Article
VL - 6
JO - Scientific Reports
JF - Scientific Reports
IS - 32317
M1 - 32317
ER -