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Yanxin Li

Publications and source records attributed to Yanxin Li.

2 recordsLinked to original sources

Automated Discrimination of Dicentric and Monocentric Chromosomes by Machine Learning-based Image Processing

Dose from radiation exposure can be estimated from dicentric chromosome (DC) frequencies in metaphase cells of peripheral blood lymphocytes. We automated DC detection by extracting features in Giemsa-stained metaphase chromosome images and classifying objects by machine learning (ML). DC detection involves i) intensity thresholded segmentation of metaphase objects, ii) chromosome separation by watershed transformation and elimination of inseparable chromosome clusters, fragments and staining debris using a morphological decision tree filter, iii) determination of chromosome width and centreline, iv) derivation of centromere candidates and v) distinction of DCs from monocentric chromosomes (MC) by ML. Centromere candidates are inferred from 14 image features input to a Support Vector Machine (SVM). 16 features derived from these candidates are then supplied to a Boosting classifier and a second SVM which determines whether a chromosome is either a DC or MC. The SVM was trained with 292 DCs and 3135 MCs, and then tested with cells exposed to either low (1 Gy) or high (2-4 Gy) radiation dose. Results were then compared with those of 3 experts. True positive rates (TPR) and positive predictive values (PPV) were determined for the tuning parameter, {sigma}. At larger {sigma}, PPV decreases and TPR increases. At high dose, for {sigma}= 1.3, TPR = 0.52 and PPV = 0.83, while at {sigma}= 1.6, the TPR = 0.65 and PPV = 0.72. At low dose and {sigma} = 1.3, TPR = 0.67 and PPV = 0.26. The algorithm differentiates DCs from MCs, overlapped chromosomes and other objects with acceptable accuracy over a wide range of radiation exposures.

Genetics

Centromere Detection of Human Metaphase Chromosome Images using a Candidate Based Method

Accurate detection of the human metaphase chromosome centromere is an critical element of cytogenetic diagnostic techniques, including chromosome enumeration, karyotyping and radiation biodosimetry. Existing image processing methods can perform poorly in the presence of irregular boundaries, shape variations and premature sister chromatid separation, which can adversely affect centromere localization. We present a centromere detection algorithm that uses a novel profile thickness measurement technique on irregular chromosome structures defined by contour partitioning. Our algorithm generates a set of centromere candidates which are then evaluated based on a set of features derived from images of chromosomes. Our method also partitions the chromosome contour to isolate its telomere regions and then detects and corrects for sister chromatid separation. When tested with a chromosome database consisting of 1400 chromosomes collected from 40 metaphase cell images, the candidate based centromere detection algorithm was able to accurately localize 1220 centromere locations yielding a detection accuracy of 87%. We also introduce a Candidate Based Centromere Confidence (CBCC) metric which indicates an approximate confidence value of a given centromere detection and can be readily extended into other candidate related detection problems.

Genetics