Volume 12, issue 9, September 2011
21 articles in this issue
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Computational and statistical approaches to analyzing variants identified by exome sequencing
Authors
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The promise and limitations of population exomics for human evolution studies
Authors (first, second and last of 4)
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Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families
Authors (first, second and last of 21)
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Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes
Authors (first, second and last of 11)
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Exome sequencing identifies a missense mutation in Isl1associated with low penetrance otitis media in dearisch mice
Authors (first, second and last of 8)
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Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia
Authors (first, second and last of 7)
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Comparison of solution-based exome capture methods for next generation sequencing
Authors (first, second and last of 14)
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SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing
Authors (first, second and last of 5)
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Comprehensive comparison of three commercial human whole-exome capture platforms
Authors (first, second and last of 14)
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First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum
Authors (first, second and last of 14)
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Effective detection of rare variants in pooled DNA samples using Cross-pool tailcurve analysis
Authors (first, second and last of 7)
