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What is Genetic Modification?
What is Genetic Modification?

Pleiotropy - MACscience
Pleiotropy - MACscience

... ability to hear • Pigmentation may play a role in maintaining fluid in ear canals ...
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MetaQuant : a new platform dealing with DNA samples
MetaQuant : a new platform dealing with DNA samples

... A new platform dealing with DNA samples to produce metagenomic analysis. A use case for big data. ...
Mamm_Genome yTrx1-2 + refs
Mamm_Genome yTrx1-2 + refs

... pseudogene could have originated approximately 18 millions years ago. If a higher mutation rate, 4.7 x 10-9 per nucleotide per year estimated for mammals (Li et al. 1987) is employed instead, the origin of the pseudogene would have been approximately 7.8 millions years ago. In any case, the inserti ...
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Analyzing Copy Number Variation in the Human Genome

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Modification of Mendelian Ratios

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...  A group of skeletal dysplasias characterized by short ribs, short limbs, polydactyly and visceral abnormalities  Lethal in the newborn period  Four types (I-IV), genes not known  Presumed AR inheritance  Diagnosed on ultrasound scan ...
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Assigned exercise

... 6. Go to ExPASy. How many annotated human genes in SwissProt and trEMBL contain the term "homeo"? Note that "*" is automatically used as prefix and suffix unless you specify otherwise. Number found: ______ . 7. What can you find out about the function of this similar gene? ...
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Copy-number variation



Copy-number variations (CNVs)—a form of structural variation—are alterations of the DNA of a genome that results in the cell having an abnormal or, for certain genes, a normal variation in the number of copies of one or more sections of the DNA. CNVs correspond to relatively large regions of the genome that have been deleted (fewer than the normal number) or duplicated (more than the normal number) on certain chromosomes. For example, the chromosome that normally has sections in order as A-B-C-D might instead have sections A-B-C-C-D (a duplication of ""C"") or A-B-D (a deletion of ""C"").This variation accounts for roughly 13% of human genomic DNA and each variation may range from about one kilobase (1,000 nucleotide bases) to several megabases in size. CNVs contrast with single-nucleotide polymorphisms (SNPs), which affect only one single nucleotide base.
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