11 research outputs found

    Ownership Characteristics of Heir Property in a Black Belt County: A Quantitative Approach

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    The existing literature identifies heir property, land held communally by heirs of someone who has died without a will, as a primary cause of land loss among African Americans and a major factor contributing to persistent poverty in the South’s demographically-defined Black Belt. Despite the importance of this form of property, little systematic research has been done to quantify the extent of heir property or the potential wealth tied up in clouded titles. This study documents the presence of more than 1,500 heir property parcels in one Alabama Black Belt county (Macon) and describes the methodological challenges involved in such research. Our analysis identified distinctive characteristics of and significant relationships between a set of key ownership variables (taxpayer location, size and value of land, structural improvements, and municipal incorporation). We argue the need to document the extent and consequences of heir property to spur action by legislators, Extension Systems across the region, and pro-bono attorneys, among others, to address the personal and economic costs associated with this form of insecure ownership

    Finishing the euchromatic sequence of the human genome

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    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
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