Karyotype AI for Precision Oncology
- URL: http://arxiv.org/abs/2211.14312v3
- Date: Thu, 19 Oct 2023 20:58:13 GMT
- Title: Karyotype AI for Precision Oncology
- Authors: Zahra Shamsi, Drew Bryant, Jacob Wilson, Xiaoyu Qu, Avinava Dubey,
Konik Kothari, Mostafa Dehghani, Mariya Chavarha, Valerii Likhosherstov,
Brian Williams, Michael Frumkin, Fred Appelbaum, Krzysztof Choromanski, Ali
Bashir, Min Fang
- Abstract summary: Efforts to automate karyotype analysis to date fell short in aberration detection.
TopViT outperformed CNN (Inception) models with >99.3% accuracy for chromosome identification.
- Score: 24.283441582734255
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Chromosome analysis is essential for diagnosing genetic disorders. For
hematologic malignancies, identification of somatic clonal aberrations by
karyotype analysis remains the standard of care. However, karyotyping is costly
and time-consuming because of the largely manual process and the expertise
required in identifying and annotating aberrations. Efforts to automate
karyotype analysis to date fell short in aberration detection. Using a training
set of ~10k patient specimens and ~50k karyograms from over 5 years from the
Fred Hutchinson Cancer Center, we created a labeled set of images representing
individual chromosomes. These individual chromosomes were used to train and
assess deep learning models for classifying the 24 human chromosomes and
identifying chromosomal aberrations. The top-accuracy models utilized the
recently introduced Topological Vision Transformers (TopViTs) with
2-level-block-Toeplitz masking, to incorporate structural inductive bias.
TopViT outperformed CNN (Inception) models with >99.3% accuracy for chromosome
identification, and exhibited accuracies >99% for aberration detection in most
aberrations. Notably, we were able to show high-quality performance even in
"few shot" learning scenarios. Incorporating the definition of clonality
substantially improved both precision and recall (sensitivity). When applied to
"zero shot" scenarios, the model captured aberrations without training, with
perfect precision at >50% recall. Together these results show that modern deep
learning models can approach expert-level performance for chromosome aberration
detection. To our knowledge, this is the first study demonstrating the
downstream effectiveness of TopViTs. These results open up exciting
opportunities for not only expediting patient results but providing a scalable
technology for early screening of low-abundance chromosomal lesions.
Related papers
- Supervised Contrastive Learning for Fine-grained Chromosome Recognition [7.427070103487921]
Chromosome recognition is an essential task in karyotyping, which plays a vital role in birth defect diagnosis and biomedical research.
Existing classification methods face significant challenges due to the inter-class similarity and intra-class variation of chromosomes.
We propose a supervised contrastive learning strategy that is tailored to train model-agnostic deep networks for reliable chromosome classification.
arXiv Detail & Related papers (2023-12-12T06:12:21Z) - Masked conditional variational autoencoders for chromosome straightening [14.665481276886194]
Karyotyping is of importance for detecting chromosomal aberrations in human disease.
chromosomes easily appear curved in microscopic images, which prevents cytogeneticists from analyzing chromosome types.
We propose a framework for chromosome straightening, which comprises a preliminary processing algorithm and a generative model.
arXiv Detail & Related papers (2023-06-25T05:11:41Z) - Improving Deep Facial Phenotyping for Ultra-rare Disorder Verification
Using Model Ensembles [52.77024349608834]
We analyze the influence of replacing a DCNN with a state-of-the-art face recognition approach, iResNet with ArcFace.
Our proposed ensemble model achieves state-of-the-art performance on both seen and unseen disorders.
arXiv Detail & Related papers (2022-11-12T23:28:54Z) - Few-Shot Meta Learning for Recognizing Facial Phenotypes of Genetic
Disorders [55.41644538483948]
Automated classification and similarity retrieval aid physicians in decision-making to diagnose possible genetic conditions as early as possible.
Previous work has addressed the problem as a classification problem and used deep learning methods.
In this study, we used a facial recognition model trained on a large corpus of healthy individuals as a pre-task and transferred it to facial phenotype recognition.
arXiv Detail & Related papers (2022-10-23T11:52:57Z) - Chromosome Segmentation Analysis Using Image Processing Techniques and
Autoencoders [0.0]
Chromosome analysis and identification from metaphase images is a critical part of cytogenetics based medical diagnosis.
Process of identification of chromosomes from metaphase is a tedious one and requires trained personnel and several hours to perform.
We propose a method to automate the process of detection and segmentation of chromosomes from a given metaphase image.
arXiv Detail & Related papers (2022-09-12T17:06:42Z) - Seamless Iterative Semi-Supervised Correction of Imperfect Labels in
Microscopy Images [57.42492501915773]
In-vitro tests are an alternative to animal testing for the toxicity of medical devices.
Human fatigue plays a role in error making, making the use of deep learning appealing.
We propose Seamless Iterative Semi-Supervised correction of Imperfect labels (SISSI)
Our method successfully provides an adaptive early learning correction technique for object detection.
arXiv Detail & Related papers (2022-08-05T18:52:20Z) - Deep Learning based Automatic Detection of Dicentric Chromosome [0.0]
This paper proposes a completely data driven framework which requires minimum intervention of field experts.
Images are extracted from YOLOv4 based on the protocols described by WHO-BIODOSNET.
We report an accuracy in dicentric identification of 94.33% on a 1:1 split of Dicentric and Monocentric Chromosomes.
arXiv Detail & Related papers (2022-04-17T15:11:13Z) - Assessing glaucoma in retinal fundus photographs using Deep Feature
Consistent Variational Autoencoders [63.391402501241195]
glaucoma is challenging to detect since it remains asymptomatic until the symptoms are severe.
Early identification of glaucoma is generally made based on functional, structural, and clinical assessments.
Deep learning methods have partially solved this dilemma by bypassing the marker identification stage and analyzing high-level information directly to classify the data.
arXiv Detail & Related papers (2021-10-04T16:06:49Z) - Wide & Deep neural network model for patch aggregation in CNN-based
prostate cancer detection systems [51.19354417900591]
Prostate cancer (PCa) is one of the leading causes of death among men, with almost 1.41 million new cases and around 375,000 deaths in 2020.
To perform an automatic diagnosis, prostate tissue samples are first digitized into gigapixel-resolution whole-slide images.
Small subimages called patches are extracted and predicted, obtaining a patch-level classification.
arXiv Detail & Related papers (2021-05-20T18:13:58Z) - Adversarial Multiscale Feature Learning for Overlapping Chromosome
Segmentation [6.180155406275231]
Chromosome karyotype analysis is of great clinical importance in the diagnosis and treatment of diseases.
Due to the strip shape of the chromosomes, they easily get overlapped with each other when imaged.
We present an adversarial multiscale feature learning framework to improve the accuracy and adaptability of overlapping chromosome segmentation.
arXiv Detail & Related papers (2020-12-22T06:04:22Z) - 1-D Convlutional Neural Networks for the Analysis of Pupil Size
Variations in Scotopic Conditions [79.71065005161566]
1-D convolutional neural network models are trained for classification of short-range sequences.
Model provides prediction with high average accuracy on a hold out test set.
arXiv Detail & Related papers (2020-02-06T17:25:37Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.