scholarly journals COMPUTER-ORIENTED ANALYSIS OF HUMAN CHROMOSOMES IV. DEOXYRIBONUCLEIC ACID-BASED CENTROMERIC INDEX

1974 ◽  
Vol 22 (7) ◽  
pp. 554-560 ◽  
Author(s):  
MORTIMER L. MENDELSOHN ◽  
DEBORAH E. BENNETT ◽  
ELLIOT BOGART ◽  
BRIAN H. MAYALL

A density-oriented semiautomatic method to estimate centromeric index is described and tested on 4611 human chromosomal images. Chromosomes are stained for deoxyribonucleic acid with gallocyanin-chrome alum and their optical density is recorded by a digital scanning microscope. Shape information in the chromosome boundary leads to a provisional centromeric position. The chromosome is divided into strips 0.25-0.35 µm wide paralleling the centromere. Optical density is integrated within each strip, strips are assembled into a density profile and the definitive centromere is located at the major local minimum in the profile. Centromeric index (large arm:total) is based on optical density or area. A test set of 4611 chromosomal images is based on over 2500 chromosomes (56 metaphase cells from six individuals) and excludes overlapped and excessively bent chromosomes. The program fails in 1.2% of the test images. Standard deviation within chromosome groups of centromeric index based on density is 0.024 and replication error is 0.016. Systematic differences between area-based and density-based measurements are observed and interpreted.


Nature ◽  
1965 ◽  
Vol 208 (5009) ◽  
pp. 486-487 ◽  
Author(s):  
A. WARD


Author(s):  
Hong-Chou Lyu ◽  
Hsing-Cheng Yu ◽  
Kuen-Chiuan Cheng ◽  
Yuan-Chin Lee ◽  
Jau-Jiu Ju


Science ◽  
1973 ◽  
Vol 179 (4078) ◽  
pp. 1126-1129 ◽  
Author(s):  
M. L. Mendelsohn ◽  
B. H. Mayall ◽  
E. Bogart ◽  
D. H. Moore ◽  
B. H. Perry


1974 ◽  
Vol 22 (7) ◽  
pp. 478-491 ◽  
Author(s):  
SAMUEL A. LATT

Fluorescence of the dye 33258 Hoechst, when bound to chromosomes, is partially quenched by the incorporation of 5-bromodeoxyuridine into chromosomal deoxyribonucleic acid (DNA). This effect allows microfluorometric analysis of DNA synthesis. Metaphase chromosomes from cultured human leukocytes which have incorporated 5-bromodeoxyuridine for a portion of the DNA synthesis period exhibit reduced 33258 Hoechst fluorescence in 5-bromodeoxyuridine-containing regions. Regions synthesizing DNA during a particular interval can thus be highlighted by the appropriate protocol of 5-bromodeoxyuridine administration. Chromosomes from cells which have replicated twice in medium containing 5-bromodeoxyuridine exhibit one brightly and one dully fluorescing chromatid, reflecting incorporation of 5-bromodeoxyuridine into one or two chains of chromatid DNA, respectively. Sister chromatid exchanges, evident as sharply demarcated reciprocal alterations in fluorescence along chromosomes, can be located relative to quinacrine banding patterns. This fluorometric approach should be useful in many instances as a convenient, high resolution alternative to autoradiography.



1969 ◽  
Vol 157 (1 Data Extracti) ◽  
pp. 376-392 ◽  
Author(s):  
Mortimer L. Mendelsohn ◽  
David A. Hungerford ◽  
Brian H. Mayall ◽  
Benson Perry ◽  
Thomas Conway ◽  
...  


2011 ◽  
Author(s):  
Hong-Chou Lyu ◽  
Hsing-Cheng Yu ◽  
Kuen-Chiuan Cheng ◽  
Yuan-Chin Lee ◽  
Jau-Jiu Ju


1990 ◽  
Vol 85 (1) ◽  
pp. 41-48 ◽  
Author(s):  
Gert A. Boschman ◽  
Wim Rens ◽  
Eric Manders ◽  
Carel van Oven ◽  
Gerrit W. Barendsen ◽  
...  


1977 ◽  
Vol 39 (2) ◽  
pp. 169-175 ◽  
Author(s):  
V. A. Benyush ◽  
V. G. Luckash ◽  
A. V. Shtannikov


1994 ◽  
Vol 57 (6) ◽  
pp. 486-489 ◽  
Author(s):  
K. R. MATTHEWS ◽  
S. P. OLIVER

Genomic deoxyribonucleic acid (DNA) of Staphylococcus species was analyzed by polymerase chain reaction-based (PCR-based) DNA fingerprinting to distinguish between species. A total of 123 staphylococci isolated from bovine mammary secretions, and nine type strains representing eight species were evaluated. Amplified DNA fragments were categorized as either primary, secondary or variable fragments. Primary [optical density > 0.3 absorbance units (AU)] and secondary fragments (optical density > 0.12 AU) were observed in all isolates within a species. Infrequent DNA fragments were designated as variable fragments (optical density > 0.12 AU). Profiles were discrete and reproducible for each species. A simple identification scheme was developed based on the occurrence of primary and secondary DNA fragments for a species. A computer integrated scanning laser densitometer was utilized to store, retrieve, compare and evaluate DNA fingerprint profiles. This permitted rapid and accurate evaluation of staphylococcal isolates. Results of this study suggest that PCR-based DNA fingerprinting is suitable for typing Staphylococcus species of bovine origin. This technique could be of value to researchers and clinicians involved in the study of bacteria isolated from food, humans and animals.



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