32 research outputs found

    Finishing the euchromatic sequence of the human genome

    Get PDF
    The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∌99% of the euchromatic genome and is accurate to an error rate of ∌1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

    How Negative Sentiment towards Muslim Americans Predicts Support for Trump in the 2016 Presidential Election

    No full text
    Replication files for "How Negative Sentiment towards Muslim Americans Predicts Support for Trump in the 2016 Presidential Election

    Replication Data for: Labels vs. Pictures: Treatment-Mode Effects in Experiments About Discrimination

    No full text
    This is replication data and code for "Labels vs. Pictures: Treatment-Mode Effects in Experiments About Discrimination" published in Political Analysis

    Racially Polarized Voting

    Get PDF
    Whether voting is racially polarized has for the last generation been the linchpin question in vote dilution cases under the core, nationally applicable provision of the Voting Rights Act. The polarization test is supposed to be clear-cut (“manageable”), diagnostic of liability, and free of strong racial assumptions. Using evidence from a random sample of vote dilution cases, we argue that these objectives have not been realized in practice and, further, that they cannot be realized under current conditions. The roots of the problem are twofold: (1) the widely shared belief that polarization determinations should be grounded on votes cast in actual elections; and (2) normative disagreement, often covert, about the meaning of racial vote dilution. We argue that the principal normative theories of vote dilution have conflicting implications for the racial-polarization test. We also show that votes are related only contingently to the political preferences that the polarization inquiry is supposed to reveal and, further, that the estimation of candidates’ vote shares by racial group from ballots cast in actual elections depends on racialhomogeneity assumptions similar to those that the Supreme Court has disavowed. Our analysis casts serious doubt on the notion—promoted in dicta by the Supreme Court and supported by prominent commentators—that courts should establish bright-line vote-share cutoffs for “legally significant” racial polarization. The courts would do better to screen vote dilution claims using either evidence of preference polarization derived from surveys or nonpreference evidence of minority political incorporation
    corecore