Excel Table providing the collected data, together with a Excel-based tool to extract specific parts of the data.

The annual Retail store data CD-ROM is an easy-to-use tool for quickly discovering retail trade patterns and trends. The current product presents results from the 1999 and 2000 Annual Retail Store and Annual Retail Chain surveys. This product contains numerous cross-classified data tables using the North American Industry Classification System (NAICS). The data tables provide access to a wide range of financial variables, such as revenues, expenses, inventory, sales per square footage (chain stores only) and the number of stores. Most data tables contain detailed information on industry (as low as 5-digit NAICS codes), geography (Canada, provinces and territories) and store type (chains, independents, franchises). The electronic product also contains survey metadata, questionnaires, information on industry codes and definitions, and the list of retail chain store respondents.

Excel spreadsheets by species (4 letter code is abbreviation for genus and species used in study, year 2010 or 2011 is year data collected, SH indicates data for Science Hub, date is date of file preparation). The data in a file are described in a read me file which is the first worksheet in each file. Each row in a species spreadsheet is for one plot (plant). The data themselves are in the data worksheet. One file includes a read me description of the column in the date set for chemical analysis. In this file one row is an herbicide treatment and sample for chemical analysis (if taken). This dataset is associated with the following publication: Olszyk , D., T. Pfleeger, T. Shiroyama, M. Blakely-Smith, E. Lee , and M. Plocher. Plant reproduction is altered by simulated herbicide drift toconstructed plant communities. ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY. Society of Environmental Toxicology and Chemistry, Pensacola, FL, USA, 36(10): 2799-2813, (2017).

The supply and use tables focus on measuring the productive structure of the economy. They trace production of commodities by domestic industries, combined with imports, through their use as intermediate inputs or as final consumption, investment or exports. The system provides a measure of value added by industry-total output (or sales) less intermediate inputs. These tables can be used to calculate economy-wide gross domestic product (GDP) either directly, by summing value added over the industries, or indirectly, by summing to the economy-wide cost of primary inputs (income-based GDP) or by computing the grand total of the flow of products into final demand categories (expenditure-based GDP)-the link to the national income and expenditure accounts. While the supply and use tables closely reflect actual economic transactions, certain analytical and modeling purposes, however, require symmetric industry-by-industry tables. These symmetric industry-by-industry tables are referred to as input-output tables. The input-output tables show the inter-industry transactions, that is, all purchases of an industry from all other industries, including expenditures on imports and inventory withdrawals, as well as all expenditures on primary inputs. Similarly, the symmetric final demand table shows all purchases by a final demand category from all other industries, including expenditures on imports and inventory withdrawals as well as all expenditures on indirect taxes. The input-output tables allow the analyst to explore "what if?" questions at a fairly detailed level, exploring the impact of exogenous changes in final demand on output while taking account of the interdependencies between different industries and regions of the economy and the leakages to imports and taxes. For example, such models might be used to study the question: "If Canadian oil and gas exports doubled, what industries would be most affected and in which provinces"? The use of an input-output model to address such a question would permit the estimation of indirect, and possibly also some of the induced effects of a demand shock of this nature, and the calculation of the corresponding multipliers. Input-output models were originally developed in the 1930s by Wassily Leontief, a Russian-American who earned the Nobel Prize in Economic Sciences for this work in 1973. His models were inspired by earlier studies by François Quesnay on the "Tableau économique" in 1758 and Léon Walras on general equilibrium theory in 1874. Leontief's models simplified earlier formulations by assuming that the proportions of industry inputs to industry outputs are fixed in the short-term, with no substitutability among any of the intermediate or factor inputs.

What is IPGOD? The Intellectual Property Government Open Data (IPGOD) includes over 100 years of registry data on all intellectual property (IP) rights administered by IP Australia. It also has derived information about the applicants who filed these IP rights, to allow for research and analysis at the regional, business and individual level. This is the 2019 release of IPGOD. # How do I use IPGOD? IPGOD is large, with millions of data points across up to 40 tables, making them too large to open with Microsoft Excel. Furthermore, analysis often requires information from separate tables which would need specialised software for merging. We recommend that advanced users interact with the IPGOD data using the right tools with enough memory and compute power. This includes a wide range of programming and statistical software such as Tableau, Power BI, Stata, SAS, R, Python, and Scalar. # IP Data Platform IP Australia is also providing free trials to a cloud-based analytics platform with the capabilities to enable working with large intellectual property datasets, such as the IPGOD, through the web browser, without any installation of software. IP Data Platform # References The following pages can help you gain the understanding of the intellectual property administration and processes in Australia to help your analysis on the dataset. * Patents * Trade Marks * Designs * Plant Breeder’s Rights # Updates ### Tables and columns Due to the changes in our systems, some tables have been affected. * We have added IPGOD 225 and IPGOD 325 to the dataset! * The IPGOD 206 table is not available this year. * Many tables have been re-built, and as a result may have different columns or different possible values. Please check the data dictionary for each table before use. ### Data quality improvements Data quality has been improved across all tables. * Null values are simply empty rather than '31/12/9999'. * All date columns are now in ISO format 'yyyy-mm-dd'. * All indicator columns have been converted to Boolean data type (True/False) rather than Yes/No, Y/N, or 1/0. * All tables are encoded in UTF-8. * All tables use the backslash \ as the escape character. * The applicant name cleaning and matching algorithms have been updated. We believe that this year's method improves the accuracy of the matches. Please note that the "ipa_id" generated in IPGOD 2019 will not match with those in previous releases of IPGOD.

This repository includes supplemental results files in Excel format from the following publication:White et al., (2024) "Alcohol Use Disorder-Associated DNA Methylation in the Nucleus Accumbens and Dorsolateral Prefrontal Cortex"

The supplementary materials include the R script used to perform the hierarchical clustering of structural variants detected by six variants callers, Figures S1 - S17, Tables S1 - S6, the assembly of AcMNPV, IIV6, IIV31 and HCMV genomes as well as there associated gff annoation files.

The supplementary tables contain information on the genomic structural variants we have detected in populations of four large double stranded DNA viruses: the baculovirus AcMNPV, the iridoviruses IIV6 and IIV31 and the herpesvirus HCMV. The tables are provided in .xlsx format and can be open in Excel.

This file is formatted as an Excel table (.xlsx format). Data table of preclassified tourism articles based on research methodology. In the data table, four columns are included:

Warning: Large file size (over 1GB). Each monthly data set is large (over 4 million rows), but can be viewed in standard software such as Microsoft WordPad (save by right-clicking on the file name and selecting 'Save Target As', or equivalent on Mac OSX). It is then possible to select the required rows of data and copy and paste the information into another software application, such as a spreadsheet. Alternatively, add-ons to existing software, such as the Microsoft PowerPivot add-on for Excel, to handle larger data sets, can be used. The Microsoft PowerPivot add-on for Excel is available from Microsoft http://office.microsoft.com/en-gb/excel/download-power-pivot-HA101959985.aspx Once PowerPivot has been installed, to load the large files, please follow the instructions below. Note that it may take at least 20 to 30 minutes to load one monthly file. 1. Start Excel as normal 2. Click on the PowerPivot tab 3. Click on the PowerPivot Window icon (top left) 4. In the PowerPivot Window, click on the "From Other Sources" icon 5. In the Table Import Wizard e.g. scroll to the bottom and select Text File 6. Browse to the file you want to open and choose the file extension you require e.g. CSV Once the data has been imported you can view it in a spreadsheet. What does the data cover? General practice prescribing data is a list of all medicines, dressings and appliances that are prescribed and dispensed each month. A record will only be produced when this has occurred and there is no record for a zero total. For each practice in England, the following information is presented at presentation level for each medicine, dressing and appliance, (by presentation name): - the total number of items prescribed and dispensed - the total net ingredient cost - the total actual cost - the total quantity The data covers NHS prescriptions written in England and dispensed in the community in the UK. Prescriptions written in England but dispensed outside England are included. The data includes prescriptions written by GPs and other non-medical prescribers (such as nurses and pharmacists) who are attached to GP practices. GP practices are identified only by their national code, so an additional data file - linked to the first by the practice code - provides further detail in relation to the practice. Presentations are identified only by their BNF code, so an additional data file - linked to the first by the BNF code - provides the chemical name for that presentation.

An Excel file detailing the identified academic literature based on the research process described in the publication and research protocol.

The Immunoglobulin fold (Ig-fold) is found in proteins from all domains of life and represents the most populous fold in the human genome, with current estimates ranging from 2 to 3% of protein coding regions. That proportion is much higher in the surfaceome where Ig and Ig-like domains orchestrate cell-cell recognition, adhesion and signaling. The ability of Ig-domains to reliably fold and self-assemble through highly specific interfaces represents a remarkable property of these domains, making them key elements of molecular interaction systems: the immune system, the nervous system, the vascular system and the muscular system. We define a universal residue numbering scheme, common to all domains sharing the Ig-fold in order to study the wide spectrum of Ig-domain variants constituting the Ig-proteome and Ig-Ig interactomes at the heart of these systems. The “IgStrand numbering scheme” enables the identification of Ig structural proteomes and interactomes in and between any species, and comparative structural, functional, and evolutionary analyses. We review how Ig-domains are classified today as topological and structural variants and highlight the “Ig-fold irreducible structural signature” shared by all of them. The IgStrand numbering scheme lays the foundation for the systematic annotation of structural proteomes by detecting and accurately labeling Ig-, Ig-like and Ig-extended domains in proteins, which are poorly annotated in current databases and opens the door to accurate machine learning. Importantly, it sheds light on the robust Ig protein folding algorithm used by nature to form beta sandwich supersecondary structures. The numbering scheme powers an algorithm implemented in the interactive structural analysis software iCn3D to systematically recognize Ig-domains, annotate them and perform detailed analyses comparing any domain sharing the Ig-fold in sequence, topology and structure, regardless of their diverse topologies or origin. The scheme provides a robust fold detection and labeling mechanism that reveals unsuspected structural homologies among protein structures beyond currently identified Ig- and Ig-like domain variants. Indeed, multiple folds classified independently contain a common structural signature, in particular jelly-rolls. Examples of folds that harbor an “Ig-extended” architecture are given. Applications in protein engineering around the Ig-architecture are straightforward based on the universal numbering.