SNP and copy number variation Databases

SNP and copy number variation Databases

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Gene Duplication: most important source of new genes; can result from unequal crossing-over: a chance mistake caused by the proteins involved in managing recombination during meiosis; homologous chromosomes don't synapse correctly during prophase of meiosis I & results in a chromosome with a redundant stretch of DNA; has an extra copy; because 1 copy produces normal product, the other is free to accumulate mutations w/o consequences to phenotype; might change function to become new gene

Gene Duplication: most important source of new genes; can result from unequal crossing-over: a chance mistake caused by the proteins involved in managing recombination during meiosis; homologous chromosomes don't synapse correctly during prophase of meiosis I & results in a chromosome with a redundant stretch of DNA; has an extra copy; because 1 copy produces normal product, the other is free to accumulate mutations w/o consequences to phenotype; might change function to become new gene

Signature of backward replication slippage at the copy number variation junction

Signature of backward replication slippage at the copy number variation junction

Genetics in Medicine - Abstract of article: Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

Genetics in Medicine - Abstract of article: Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

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8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families

8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families

CD Genomics provides a number of options for those looking to perform copy number variation (CNV) analysis on several different microarray platforms depending on the organism, starting material and size of your project. http://www.cd-genomics.com/CNV-Analysis-Service.html

CD Genomics provides a number of options for those looking to perform copy number variation (CNV) analysis on several different microarray platforms depending on the organism, starting material and size of your project. http://www.cd-genomics.com/CNV-Analysis-Service.html

Silver Wings intaglio print with chine colle is printed on archival blue pescia paper, with thai kozo using oil based inks. Signed, titled, and numbered by the artist. Each copy is uniquely manually printed, some minute variations exist. Paper size approximately 11.35 x 9.5 .  This artwork is not a digitally reproduced print. It is 100% made by me!  To make my traditionally crafted intaglio prints or etchings, I hand draw my original designs on a resin coated metal plate. Once drawn, the…

Silver Wings intaglio print with chine colle is printed on archival blue pescia paper, with thai kozo using oil based inks. Signed, titled, and numbered by the artist. Each copy is uniquely manually printed, some minute variations exist. Paper size approximately 11.35 x 9.5 . This artwork is not a digitally reproduced print. It is 100% made by me! To make my traditionally crafted intaglio prints or etchings, I hand draw my original designs on a resin coated metal plate. Once drawn, the…

Mitochondrial DNA copy number variation across human cancers

Mitochondrial DNA copy number variation across human cancers

RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene

RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene

A numbers game – Copy Number Variations in schizophrenia

A numbers game – Copy Number Variations in schizophrenia

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