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Your search keyword '"Rashida Anwar"' showing total 2 results
Start Over Author "Rashida Anwar" Publisher public library of science (plos)
2 results on '"Rashida Anwar"'

1. Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype.

Author

Ian M Carr, Christine P Diggle, Kamron Khan, Chris Inglehearn, Martin McKibbin, David T Bonthron, Alexander F Markham, Rashida Anwar, Angus Dobbie, Sergio D J Pena, and Manir Ali

Subjects
Medicine, Science
Abstract

Whilst the majority of inherited diseases have been found to be caused by single base substitutions, small insertions or deletions (

Published
2012
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2. Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype

Author

Kamron N. Khan, Christine P. Diggle, Sérgio D.J. Pena, Rashida Anwar, Manir Ali, David T. Bonthron, Ian M. Carr, Angus Dobbie, Alexander F. Markham, Chris F. Inglehearn, Martin McKibbin, and Adamovic, T

Subjects
Male, DNA Copy Number Variations, Microarray, Microarrays, Copy number analysis, lcsh:Medicine, Loss of Heterozygosity, Biology, Polymorphism, Single Nucleotide, Genome, Cytogenetics, Chromosomal Disorders, Genome Analysis Tools, Genetics, Humans, Genetic Predisposition to Disease, Genetic Testing, Genetic variability, Copy-number variation, lcsh:Science, Aniridia, Genotyping, Genetic Association Studies, Oligonucleotide Array Sequence Analysis, Chromosome Aberrations, Family Health, Clinical Genetics, Linkage Maps, Multidisciplinary, Genome, Human, lcsh:R, Chromosome Mapping, Reproducibility of Results, Computational Biology, Chromosomal Deletions and Duplications, Human Genetics, Genomics, Phenotype, Pedigree, Cytogenetic Analysis, Medicine, lcsh:Q, Female, DNA microarray, Software, Research Article
Abstract

Whilst the majority of inherited diseases have been found to be caused by single base substitutions, small insertions or deletions (

Published
2012

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