Very happy to share our new @biorxivpreprint showing that phenotypic correlations between in vitro fertilization (#IVF) sibling embryos provide predictive value regarding an embryo’s future implantation potential!
We started by showing that embryos from the same cohort are phenotypically correlated
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The implantation potential of transferred embryos was associated with the phenotype of their non-transferred “sibling”. Siblings’ phenotypes contribute to image-based machine learning embryo implantation prediction for models trained with morphology/morphokinetic features!
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The fraction of sibling embryos reaching blastulation came up as the most important feature for prediction of implantation outcome in a model trained with morphology, morphokinetics, oocyte age & cohort features! 5/10 top features were attributed to the cohort’s siblings!
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Embryos that were “rescued” by the cohort features, meaning correctly classified only by the classifier that had access to cohort information, relied on the two top ranked cohort features, and *only* “rescued” implanted embryos erroneously classified as non-implanted 🤔
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We think that the model was able to correct negative-to-positive but not positive-to-negative predictions because failed implantations are caused either by defected embryos or maternal clinical properties translating to ambiguous labels that mislead the classifier
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Altogether, we suggest that the #ML uncertainty in the transferred embryo is reduced by noise reduction from the multiple correlated (sibling) instances.
Or in other words, @Giannis_An34 could be predicted to be a basketball player according to his siblings 😉
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This is an example of semi-supervised learning: a small fraction of labeled (transferred embryos) and vast unlabeled (non-transferred siblings) observations. Unlike traditional semi-supervised learning, here the unlabeled and labeled observations are associated.
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In summary, inclusion of cohort features contribute to machine learning models trained with embryo-derived features. Since the siblings’ data are routinely collected, incorporating them in #AI-driven embryo implantation prediction can have direct implications in the clinic!
Very excited to share my last postdoc project at the @gdanuser1 lab where we "reverse engineered" a neural network to identify the cellular properties that distinguish aggressive and less aggressive metastatic melanoma!
This was a team effort that started back in 2014 (!), asking can we predict metastatic potential using unstructured image properties from live label-free cell images?
Special thanks to Andrew Jamieson, @ErikWelf, and @TechnicolorDres who took critical roles in this project!
They xenografted patient-derived stage III melanoma metastases in NSG mice and correlated the mice and the human prognosis – progression to widespread metastases in distant organs.