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Showing 1–3 of 3 results
Advanced filters: Author: Paula Rausch Clear advanced filters

  • JaBbA v1 pinpoints the ‘loose ends’ of large (>10-kb) unmapped structural variants in short-read DNA sequencing, suggesting that about 90% of cancer chromosomal alterations outside centromeres are resolvable with short reads and that long reads will primarily improve calling of smaller somatic variants.

    • Zi-Ning Choo
    • Julie M. Behr
    • Marcin Imieliński
    ResearchOpen Access
    Nature Genetics
    Volume: 55, P: 2139-2148

  • Many US federal agencies apply principles from risk communication science across a wide variety of hazards. In so doing, they identify key research and practice gaps that, if addressed, could help better serve the nation’s communities and greatly enhance practice, research, and policy development.

    • William M. P. Klein
    • Alycia K. Boutté
    • William T. Riley
    Comments & Opinion
    Nature Human Behaviour
    Volume: 5, P: 411-413

  • Comprehensive factor analysis of core diagnostic features provides insights into the complex genetic architecture underlying phenotypic heterogeneity in autism.

    • Varun Warrier
    • Xinhe Zhang
    • Simon Baron-Cohen
    ResearchOpen Access
    Nature Genetics
    Volume: 54, P: 1293-1304