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End-To-End Chromosome Karyotyping with Data Augmentation Using GAN

International Conference on Information Photonics, 2018
Classifying 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

Digital karyotyping

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
openaire   +2 more sources

The karyotype of blastic crisis

Cancer Genetics and Cytogenetics, 1987
The 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
openaire   +4 more sources

Embryonic karyotype in recurrent miscarriage with parental karyotypic aberrations

Fertility and Sterility, 2006
To 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
openaire   +3 more sources

The karyotype of the mouse

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.
openaire   +3 more sources

Karyotype of the Fox

Nature, 1964
THROUGH work with short-term cultures of leucocytes from peripheral blood according to the phytohaemagglutinin method, the opportunity arose to examine the chromosome complement of the red fox (Vulpes vulpes Lin.). As no description of the chromosome morphology has previously been published, these observations are of some interest.
openaire   +3 more sources

Karyotyping of Amoeba proteus

Cell and Tissue Biology, 2017
In this paper, the protocol which we have developed to get satisfactory spreads of Amoeba proteus mitotic chromosomes is presented, and the process of karyotyping this amoeba species is described. This protocol allows obtaining of extended chromosomic with repeatable chromomeres pattern in individual chromosomes.
A. L. Yudin   +4 more
openaire   +3 more sources

Karyotyping Methods for Fungi

2011
Pulsed field gel electrophoresis enables separation of fungal chromosomes up to several megabases and is a worthwhile tool for fungal karyotyping. The germ tube burst method is a technique to separate fungal chromosomes of any size for chromosome number determination as well as in situ hybridization.
Mehrabi, R.   +4 more
openaire   +2 more sources

Coleoptera Karyotype Database

The Coleopterists Bulletin, 2015
Blackmon, Heath, Demuth, Jeffery P. (2015): Coleoptera Karyotype Database. The Coleopterists Bulletin 69 (1): 174-175, DOI: 10.1649/0010-065X-69.1.174, URL: http://dx.doi.org/10.1649/0010-065x-69.1 ...
Blackmon, Heath, Demuth, Jeffery P.
openaire   +3 more sources

Karyotyping Techniques of Chromosomes: A Survey

, 2015
— Chromosome analysis is used by clinicians for the early detection, prognosis and treatment evaluation of genetic disorders like leukaemia, Down syndrome etc. The detection is done with the help of karyotypes.
Remya R S Revathy M Nair
semanticscholar   +1 more source

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