Loading ...
cytogenetic techniques such as fluorescent in situ hybridization , comparative genomic hybridization , array comparative genomic hybridization , end - sequence profiling and by virtual karyotyping with SNP arrays(passive) can be discovered byCopy number variation
random duplications and losses in repeat regions(passive) caused byCopy number variations
large insertion , deletion or duplication(passive) caused bycopy number variation ( CNV
large insertions and deletions(passive) caused bycopy number variation ( CNV )
Enzymes involved in copying and editing DNA during cell division may snip out , reinsert or make too many copies of stretches of the genomecreatingcopy number variations
Using a sister chromatid as repair is not a fool - proof backup as the surrounding DNA information of the n and n+1 repeat is virtually the sameleadingto copy number variation
an overview for a new method we have been developingto discovercopy number variations ( CNV
i ≤ n , 1 ≤ j ≤ w. Segmentation over multiple samples Insertions , deletions or duplicationscausingcopy number variations
either the duplication or deletion of a gene segment within a given chromosome(passive) is caused byCopy number variation
either duplication ( or insertion ) of a large genomic segment multiple times ... or may be characterized by the deletion of a large DNA segment(passive) is caused byCopy number variation
most likely(passive) are ... causedcopy number variations
losses or duplications of DNA sequences(passive) caused bycopy - number variations ( CNVs
AbstractWehave discoveredcopy number variations ( CNVs
to have phenotypic consequences(passive) have been discoveredCopy number variations ( CNVS
dietary regimens(passive) triggered bycopy number variations
that were knownto causecopy number variation ( CNV
genomic rearrangement(passive) is caused byCopy number variation ( CNV
large duplications(passive) caused bycopy - number variation
In ascertaining whether reprogrammingdoes ... contributeto copy number variation
the genome rearrangement(passive) causing byCopy number variation
losses and duplications of stretches of dna at sites across the genome(passive) is caused bycopy number variation
changes to complete genome duplication(passive) caused solely bycopy number variation
many gene gain and loss eventshave causedcopy number variation
Alu - mediated rearrangements(passive) caused bycopy number variations
genomic instabilityleadingto copy number variation
techniques including fluorescent in situ hybridization , comparative genomic hybridization(passive) can be discovered byCopy number variation
single genes(passive) caused bycopy number variations ]
6 CrossRef 7 Jacob L. Steenwyk , John S. Soghigian , John R. Perfect , John G. GibbonscontributesCopy number variation
gene rearrangementsleadingto copy number variation
American geneticist Calvin Bridgesdiscoveredcopy number variation
genomic deletions(passive) caused bycopy number variation
cytogeneticCytogeneticsCytogenetics(passive) can be discovered byCopy number variation
current models of the mechanismscausecopy number variation
the mutational mechanismsleadingto copy number variation
in reduced GENE DOSAGE due to any loss - of - function mutationresultsin reduced GENE DOSAGE due to any loss - of - function mutation
Gene expression change(passive) caused byGene expression change
gene expression and metabolic traits in mice ... Human Molecular Genetics ... volinfluencesgene expression and metabolic traits in mice ... Human Molecular Genetics ... vol
gene expression and metabolic traits in mice Orozco , Luz D. | Cokus , Shawn J. | Ghazalpour , Anatole | Ingram - Drake , Leslie | Wang , Susanna | van Nas , Atila | Che , Nam | Araujo , Jesus A. | Pellegrini , Matteo | Lusis , Aldons J. 7influencesgene expression and metabolic traits in mice Orozco , Luz D. | Cokus , Shawn J. | Ghazalpour , Anatole | Ingram - Drake , Leslie | Wang , Susanna | van Nas , Atila | Che , Nam | Araujo , Jesus A. | Pellegrini , Matteo | Lusis , Aldons J. 7
disease relevant genes(passive) influenced bydisease relevant genes
to specific human diseases ... and ... out of curiositycontributeto specific human diseases ... and ... out of curiosity
to the variation observed in susceptibility to complex diseasescan contributeto the variation observed in susceptibility to complex diseases
in excess PMP22 protein – medalteam funresultingin excess PMP22 protein – medalteam fun
extreme tall stature Creator(scausingextreme tall stature Creator(s
to considerable diversity for B but not A haplotypes of the human KIR genes encoding NK cell receptors , Genome Res , 2012 in PressJoncker NT , Raulet DHleadsto considerable diversity for B but not A haplotypes of the human KIR genes encoding NK cell receptors , Genome Res , 2012 in PressJoncker NT , Raulet DH
to the genetic basis of diseasecontributesto the genetic basis of disease
disease - causing mutations(passive) caused bydisease - causing mutations
what proportion of genetic disease(passive) is caused bywhat proportion of genetic disease
human disease states(passive) caused byhuman disease states
Rare Kidney Disease - Health News - redOrbit HomeVideoNewsImagesHealthEducationTopicsBlogsDailyTo CauseRare Kidney Disease - Health News - redOrbit HomeVideoNewsImagesHealthEducationTopicsBlogsDaily
to human lifespan [ 6–10may ... contributeto human lifespan [ 6–10
only a few years ago ... but they are immensely importantwere discoveredonly a few years ago ... but they are immensely important
to human genetic diversity and disease susceptibility , including for cancer , schizophrenia , and other complex diseasescontributesto human genetic diversity and disease susceptibility , including for cancer , schizophrenia , and other complex diseases
significantly to human genomic variationcontributessignificantly to human genomic variation
gene expression and gene functioncan influencegene expression and gene function
to gene expression variation as wellmay contributeto gene expression variation as well
the gene expression profile variation(passive) caused bythe gene expression profile variation
these only account for about 10 per cent of the known inherited risk of developing One theory for this so - called ' missing heritability ' was(passive) may have been caused bythese only account for about 10 per cent of the known inherited risk of developing One theory for this so - called ' missing heritability ' was
22 June 2009 - by Lorna Stewart Neuroblastoma , a form of paediatric cancer which affects the nervous system(passive) may be caused by22 June 2009 - by Lorna Stewart Neuroblastoma , a form of paediatric cancer which affects the nervous system
to changes in DNA dosage contributing significantly to variation between individual human genomes and heritable traitscan leadto changes in DNA dosage contributing significantly to variation between individual human genomes and heritable traits
to autism in the next generation sequencing era by AlSagob , Maysoon and Colak , Dilek and Kayaleadingto autism in the next generation sequencing era by AlSagob , Maysoon and Colak , Dilek and Kaya
to variable degrees of fitness and/or disease predispositioncan contributeto variable degrees of fitness and/or disease predisposition
significantly to the genetic architecture of human obesitycontributessignificantly to the genetic architecture of human obesity
specific phenotypes which characterise diseases and syndromescausespecific phenotypes which characterise diseases and syndromes
to cryptic genetic variation in outbreak lineages of Cryptococcus gattii from the North American Pacific Northwest | BMC Genomics | Full Text Jacob L. Steenwyk1 , 2 , John S. Soghigian1 , 3 , John R. Perfect4 and John G. Gibbons1Emailcontributesto cryptic genetic variation in outbreak lineages of Cryptococcus gattii from the North American Pacific Northwest | BMC Genomics | Full Text Jacob L. Steenwyk1 , 2 , John S. Soghigian1 , 3 , John R. Perfect4 and John G. Gibbons1Email
85 - 93 Syndromes(passive) caused by85 - 93 Syndromes
genomic disorderscausegenomic disorders
to human genetic variation and genetic disease [ 79contributeto human genetic variation and genetic disease [ 79
inherited disease in the absence of coding - sequence alterationscould causeinherited disease in the absence of coding - sequence alterations
to gene expression alterations functionally linked to cancer33can leadto gene expression alterations functionally linked to cancer33
to human diseases and phenotypescontributeto human diseases and phenotypes
The proportion of genetic diseases(passive) caused byThe proportion of genetic diseases
Gene clue to neuroblastoma - BioNews Page URL : https://www.bionews.org.uk/page_91775 Neuroblastoma , a form of paediatric cancer which affects the nervous system(passive) may be caused byGene clue to neuroblastoma - BioNews Page URL : https://www.bionews.org.uk/page_91775 Neuroblastoma , a form of paediatric cancer which affects the nervous system
to autism in the next generation sequencing era Discovery MedicineJune 25 , 2015 Maysoon AlSagobNamik Kaya Frontiers in GeneticsDecember 18 , 2018leadingto autism in the next generation sequencing era Discovery MedicineJune 25 , 2015 Maysoon AlSagobNamik Kaya Frontiers in GeneticsDecember 18 , 2018
unexplained genetic disorderscan causeunexplained genetic disorders