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Microarray Analysis 1
Microarray Analysis 1

... Like cDNAs, but instead of using a cloned gene, design a 40-70 base probe to represent each gene Relies on genome sequence database and bioinformatics Reduces cross hybridization Cheaper and possibly more sensitive than Affy. system ...
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1 DNA PHENOTYPING: PREDICTING ANCESTRY AND PHYSICAL
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... approaches for ancestry inference, principal component analysis and statistical clustering, both of which are performed at global and regional scales. Both require a database of reference DNA samples with well-defined ancestry, and thousands of subjects have been collected from populations around th ...
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Selling Genzyme Genetics` Maternal Serum Screening Program
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Recombinant DNA technology
Recombinant DNA technology

... The isolation procedure mainly involve: DNA isolation from bacteria involves lysis of cell wall by a lysozyme enzyme then alkali denaturation treatment followed by solvents extraction (phenol/chloroform/isoamyl alcohol mixture ) which separates chromosomal DNA from plasmid DNA (remains circular shap ...
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... The isolation procedure mainly involve: DNA isolation from bacteria involves lysis of cell wall by a lysozyme enzyme then alkali denaturation treatment followed by solvents extraction (phenol/chloroform/isoamyl alcohol mixture ) which separates chromosomal DNA from plasmid DNA (remains circular shap ...
Mastit 4 Mastit 4 qPCR - Mastitis test
Mastit 4 Mastit 4 qPCR - Mastitis test

Preparation of SCRATCHY Hybrid Protein Libraries
Preparation of SCRATCHY Hybrid Protein Libraries

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... • Y chromosome: found only in males and passed from father to son; only 26 million base pairs sequenced thus far out of about 60 million • Mitochondrial DNA: found in both males and females, but passed on only by the mother to her children; 16,569 base pairs in a circle • Autosomal DNA: 44 chromosom ...
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... C) In physical maps, the distances between markers are given in megabases (Mb) where 1 Mb is approximately equal to 1 cM. D) The banding patterns of chromosomes created by different staining techniques are used in constructing cytogenetic maps. E) In genetic maps, the distances between various marke ...
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... simulate the steps involved in making multiple copies of the DNA fragment 3. To use PCR to isolate a specific gene and amplify it 4. To compare the PCR products (amplified DNA fragments) by simulating gel electrophoresis 5. To identify what DNA was obtained from suspect location “The Crime” Bonan Fu ...
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... can often be very low. Techniques used for purification of DNA from buccal cells must therefore be sensitive, reliable and ensure that the DNA obtained is suitable for relevant downstream applications such as PCR, sequencing and STR analysis. ...
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... but it was extremely difficult to find faecal samples in the bracken, grassland, and scrub habitats where reptiles and pheasants were both present. A greater success of finding reptile DNA in pheasant faeces might be obtained from collecting samples between August and September, following the birth ...
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Comparative genomic hybridization



Comparative genomic hybridization is a molecular cytogenetic method for analysing copy number variations (CNVs) relative to ploidy level in the DNA of a test sample compared to a reference sample, without the need for culturing cells. The aim of this technique is to quickly and efficiently compare two genomic DNA samples arising from two sources, which are most often closely related, because it is suspected that they contain differences in terms of either gains or losses of either whole chromosomes or subchromosomal regions (a portion of a whole chromosome). This technique was originally developed for the evaluation of the differences between the chromosomal complements of solid tumor and normal tissue, and has an improved resoIution of 5-10 megabases compared to the more traditional cytogenetic analysis techniques of giemsa banding and fluorescence in situ hybridization (FISH) which are limited by the resolution of the microscope utilized.This is achieved through the use of competitive fluorescence in situ hybridization. In short, this involves the isolation of DNA from the two sources to be compared, most commonly a test and reference source, independent labelling of each DNA sample with a different fluorophores (fluorescent molecules) of different colours (usually red and green), denaturation of the DNA so that it is single stranded, and the hybridization of the two resultant samples in a 1:1 ratio to a normal metaphase spread of chromosomes, to which the labelled DNA samples will bind at their locus of origin. Using a fluorescence microscope and computer software, the differentially coloured fluorescent signals are then compared along the length of each chromosome for identification of chromosomal differences between the two sources. A higher intensity of the test sample colour in a specific region of a chromosome indicates the gain of material of that region in the corresponding source sample, while a higher intensity of the reference sample colour indicates the loss of material in the test sample in that specific region. A neutral colour (yellow when the fluorophore labels are red and green) indicates no difference between the two samples in that location.CGH is only able to detect unbalanced chromosomal abnormalities. This is because balanced chromosomal abnormalities such as reciprocal translocations, inversions or ring chromosomes do not affect copy number, which is what is detected by CGH technologies. CGH does, however, allow for the exploration of all 46 human chromosomes in single test and the discovery of deletions and duplications, even on the microscopic scale which may lead to the identification of candidate genes to be further explored by other cytological techniques.Through the use of DNA microarrays in conjunction with CGH techniques, the more specific form of array CGH (aCGH) has been developed, allowing for a locus-by-locus measure of CNV with increased resolution as low as 100 kilobases. This improved technique allows for the aetiology of known and unknown conditions to be discovered.
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