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Sophie Roth

dblp:201/7660 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2018
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 1Graphics, computer vision, multimedia, augmented reality and games · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Artificial intelligence
1 paper
Image recognition and object detection · 100%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Medical and health informatics · 100%

Topics — the 1 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Medical and health informatics › computational pathology
cell detection and classification
0.312018
Multi-Cell Detection and Classification Using a Generative Convolutional Model · CVPR 2018

Methods — techniques the papers use, named apart from their topics

probabilistic generative model · 0.7convolutional sparse coding · 0.7convolutional dictionary learning · 0.7
YearPublicationVenuePosition
2018 Multi-Cell Detection and Classification Using a Generative Convolutional Model
abstract
Detecting, counting, and classifying various cell types in images of human blood is important in many biomedical applications. However, these tasks can be very difficult due to the wide range of biological variability and the resolution limitations of many imaging modalities. This paper proposes a new approach to detecting, counting and classifying white blood cell populations in holographic images, which capitalizes on the fact that the variability in a mixture of blood cells is constrained by physiology. The proposed approach is based on a probabilistic generative model that describes an image of a population of cells as the sum of atoms from a convolutional dictionary of cell templates. The class of each template is drawn from a prior distribution that captures statistical information about blood cell mixtures. The parameters of the prior distribution are learned from a database of complete blood count results obtained from patients, and the cell templates are learned from images of purified cells from a single cell class using an extension of convolutional dictionary learning. Cell detection, counting and classification is then done using an extension of convolutional sparse coding that accounts for class proportion priors. This method has been successfully used to detect, count and classify white blood cell populations in holographic images of lysed blood obtained from 20 normal blood donors and 12 abnormal clinical blood discard samples. The error from our method is under 6.8% for all class populations, compared to errors of over 28.6% for all other methods tested.
Florence Yellin, Benjamin D. Haeffele, Sophie Roth, René Vidal
CVPR3