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PEPAdb (Prehistoric Europe's Personal Adornment Database) is a long-term, open-ended project that aims to improve access to archaeological data online. Its website (https://pepadb.us.es) publishes and analyses datasets about prehistoric personal adornment, drawing on the results of various research projects and bibliographic references.

The importance of rivers and streams for fresh water, food, and recreation is well known, yet there is increasing evidence that degradation of running waters is at an all-time high. However, most restoration projects are small scale, and information on their implementation and outcome is not readily accessible. Here, Bernhardt et al report a synthesis of information on 37,099 projects in the National River Restoration Science Synthesis database.

Chinese American genealogy sources exist in both America and China, but finding them in China can be challenging. In America, an unintended consequence of the Chinese Exclusion Act of 1882 was the generation of voluminous government records that now benefit research on Chinese Americans by providing and confirming the names of people, of villages written in Chinese characters and romanized in English, and sometimes, remarkable photographs. In China, such work was performed at the village level. Meticulous village genealogy books (zupus) record the men in each village and contain family lineages for the villagers spanning hundreds to thousands of years; women’s names were not included. Many of these books are now digitized and available through the online Village Database. In this Research Files feature, Henry Tom introduces readers to the database and guides them on how to use it.

Library database vendors often revamp simpler interfaces of their database platforms with script-enriched interfaces to make them more attractive. Sadly, these enhancements often overlook users who rely on assistive technology, leaving electronic content difficult for this user base despite the potential of electronic materials to be easier for them to access and read than print materials. Even when providers are somewhat aware of this user group's needs there are questions about the effect of their efforts to date and whether accessibility documentation from them can be relied upon. This study examines selected vendors’ VPAT reports (Voluntary Product Accessibility Template) through a manual assessment of their database platforms to determine their overall accessibility.

Injuries are a public health crisis. Neurotrauma, a specific type of injury, is a leading cause of death and disability globally, with the largest burden in low- and middle-income countries (LMICs). However, there is a lack of quality neurotrauma-specific data in LMICs, especially at the national level. Without standard criteria for what constitutes a national registry, and significant challenges frequently preventing this level of data collection, we argue that singleinstitution or regional databases can provide significant value for context-appropriate solutions. Although granular data for larger populations and a universal minimum dataset to enable comparison remain the gold standard, we must put progress over perfection. It is critical to engage local experts to explore available data and build effective information systems to inform solutions and serve as the foundation for quality and process improvement initiatives. Other items to consider include adequate resource allocation and leveraging of technology as we work to address the persistent but largely preventable injury pandemic.

The World Health Organization (WHO) has collected information on policies on sexual, reproductive, maternal, newborn, child and adolescent health (SRMNCAH) over many years. Creating a global survey that works for every country context is a well-recognized challenge. A comprehensive SRMNCAH policy survey was conducted by WHO from August 2018 through May 2019. WHO regional and country offices coordinated with Ministries of Health and/or national institutions who completed the questionnaire. The survey was completed by 150 of 194 WHO Member States using an online platform that allowed for submission of national source documents. A validation of the responses for selected survey questions against content of the national source documents was conducted for 101 countries (67%) for the first time in the administration of the survey. Data validation draws attention to survey questions that may have been misunderstood or where there was a lot of missing data, but varying methods for validating survey responses against source documents and separate analysis of laws from policies and guidelines may have hindered the overall conclusions of this process. The SRMNCAH policy survey both provided a platform for countries to track their progress in adopting WHO recommendations in national SRMNCAH-related legislation, policies, guidelines and strategies and was used to create a global database and searchable document repository. The outputs of the SRMNCAH policy survey are resources whose importance will be enriched through policy dialogues and wide utilization. Lessons learned from the methodology used for this survey can help to improve future updates and inform similar efforts.

In an age of “Big Data” the study of the history and archaeology of religion faces an exponentially increasing quantity and range of data and scholarly interpretation. For the student and scholar alike, new tools that allow for efficient and accurate inquiry are a necessity. Here, the open-access and digital Database of Religious History (DRH) is presented as one such tool that addresses this need and is well suited for use in the classroom. In this article, we present the basic structure of the database along with a demonstration of its potential use. Following a thematic inquiry into questions concerning “high gods”, individual disciplinary-specific case studies examine applications to particular contexts across time and space. These case studies demonstrate the ways in which the DRH can test and disrupt ontologies through its ability to efficiently cross traditional disciplinary boundaries.

The National Cancer Institute Initiative in Chemical Genetics is designed to encourage the development of small molecular probes. The probes are useful for activating or inactivating protein functions, thereby providing resources that help discern the functions of gene products in normal and disease cells, as well as in tissues. This initiative includes \"ChemBank,\" a suite of informatics tools and databases aimed at promoting the development and use of chemical genetics by scientists worldwide. The information generated with such tools should provide a critical link from genomic discovery to drug development.