A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries. (1/717)

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Building a comprehensive genomic program for hepatocellular carcinoma. (2/717)

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Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study. (3/717)

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Exploring patterns and extent of bias in estimating divergence time from mitochondrial DNA sequence data in a particular lineage: a case study of salamanders (order Caudata). (4/717)

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Diverging alternative splicing fingerprints in the transforming growth factor-beta signaling pathway identified in thoracic aortic aneurysms. (5/717)

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Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome. (6/717)

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Targeted sequencing of the human X chromosome exome. (7/717)

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An atlas of tissue-specific conserved coexpression for functional annotation and disease gene prediction. (8/717)

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