Results 331 to 340 of about 142,560 (388)
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Traditional and deep‐based techniques for end‐to‐end automated karyotyping: A review
Expert Syst. J. Knowl. Eng., 2021In the field of cytogenetics, chromosome image analysis or karyotyping from metaphase images plays an imperative role in the diagnosis, prognosis and treatment assessment of different genetic disorders and cancers. This paper is a comprehensive review on
Remya Remani Sathyan +4 more
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Current Protocols in Human Genetics, 1998
AbstractRelevant portions of the new International System for Human Cytogenetic Nomenclature (ISCN 1995) have been reproduced in this appendix (with permission from Karger, the original publisher). The new rules supersede all previous rules and include guidelines for cancer cytogenetics as well as new recommendations for nomenclature when in situ ...
Christine M. Disteche, Rhona Schreck
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AbstractRelevant portions of the new International System for Human Cytogenetic Nomenclature (ISCN 1995) have been reproduced in this appendix (with permission from Karger, the original publisher). The new rules supersede all previous rules and include guidelines for cancer cytogenetics as well as new recommendations for nomenclature when in situ ...
Christine M. Disteche, Rhona Schreck
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End-To-End Chromosome Karyotyping with Data Augmentation Using GAN
International Conference on Information Photonics, 2018Classifying human chromosomes from input cell images, i.e., karyotyping, requires domain expertise and quantity of manual effort to perform. In this paper, we propose an end-to-end chromosome karyotyping method, which can automatically detect, segment ...
Yirui Wu +4 more
semanticscholar +1 more source
Nature Protocols, 2007
Detection of copy number variation in the human genome is important for identifying naturally occurring copy number polymorphisms as well as alterations that underlie various human diseases, including cancer. Digital karyotyping uses short sequence tags derived from specific genomic loci to provide a quantitative and high-resolution view of copy number
Rebecca J, Leary +3 more
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Detection of copy number variation in the human genome is important for identifying naturally occurring copy number polymorphisms as well as alterations that underlie various human diseases, including cancer. Digital karyotyping uses short sequence tags derived from specific genomic loci to provide a quantitative and high-resolution view of copy number
Rebecca J, Leary +3 more
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The karyotype of blastic crisis
Cancer Genetics and Cytogenetics, 1987The nonrandomness of chromosome clonal evolution in blastic crisis of chronic myeloid leukemia is well established, with three major changes [+8, +Ph, i(17q)] occurring alone or in combination in over 70% of the patients. The chromosome changes observed in different tissues may reveal the origin of the abnormal clones, as well as provide evidence for ...
ALIMENA, Giuliana +4 more
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Karyotypes and Karyotypic Variation of North American Vespertilionid Bats
Journal of Mammalogy, 1967(Uploaded by Plazi for the Bat Literature Project) Karyotypes of 32 species of North American vespertilionid bats are described. Individual, population, subspecific, specific, and generic karyotypic variation are discussed. The use of karyotypes as a taxonomic tool and phylogenetic indicator in bats is discussed.
James L. Patton, Robert J. Baker
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Embryonic karyotype in recurrent miscarriage with parental karyotypic aberrations
Fertility and Sterility, 2006To assesses chromosomal aberrations in the abortus in recurrent miscarriage, in the presence of parental chromosomal aberrations.Retrospective comparative cohort study.Tertiary referral unit in university hospital.One thousand one hundred eight patients with 3-16 miscarriages before 20 weeks gestation; 113 patients with and 995 without chromosomal ...
Eyal Schiff +5 more
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Chromosoma, 1971
A denaturating and renaturating technique, applied to mouse chromosomes, makes visible characteristic banding patterns by which all elements of the karyotype can be individually distinguished. The Y chromosome as a whole appears darkly stained. The X chromosome comprises 6.33% of the homogametic haploid set.
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A denaturating and renaturating technique, applied to mouse chromosomes, makes visible characteristic banding patterns by which all elements of the karyotype can be individually distinguished. The Y chromosome as a whole appears darkly stained. The X chromosome comprises 6.33% of the homogametic haploid set.
openaire +3 more sources