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Art that was entirely or partially produced by an autonomous system is referred to as generative art. An autonomous system is typically a non-human entity that is capable of making judgments on its own about aspects of a piece of art that would otherwise require direct input from the artist. We have created a GUI which lists the applications which are based on the concept of generative art. Our GUI contains applications like random password generation, abstract artworks, map generation, wallpaper generation. Password generator will provide randomly generated passwords which would be derived from the images created using image generation algorithms/scripts such as EPWT and python’s in-built random function which uses algorithms like mersenne twister, a pseudo-random number generator. This application aims to provide usefulness for old hashing algorithms which are getting obsolete day by day. Abstract artwork generator will generate random images for stimulating creativity of artists, designers, architectural and marketing firms for getting started on a new project. This generator uses general complex functions which contain scripts for different shapes and combinations. This approach is able to generate some innovative solutions and demonstrates the power of computational approach. A layout of the area with the requested coordinates and different constraints will be provided through map generating model. Wallpaper generation model will generate aesthetically pleasing wallpapers with adjustable features.

Condyloma acumianata is one of the most common virally transmitted diseases. Its prevalence has increased many fold throughout the world. Because all the currently available treatments yield low cure rates with side effects, the search for a new alternative continues. Topically, 5-fluorouracil (5-FU) has been in used for many years to treat various skin diseases. When applied topically in condyloma acuminata, 5-FU results in low cure rates with high recurrences. Therefore, intralesional 5% 5-FU is being evaluated to determine its therapeutic efficacy in condyloma acuminata.

Probiotics are live microbial food supplements that are beneficial to the host health when administered in adequate amounts. Probiotics do have an exciting concept in digestive functions, but these live microbes have wider applicability as evidenced by gut-brain-skin axis theory given 80years back. However, the details regarding use of probiotics for dermatological indications ranging from atopic dermatitis to acne and sexually transmitted infections is dispersed in the literature, herein we have tried to focus all under one heading. Overall, probiotics seem to be promising and safe therapeutic modality, but the evidence as of now, from the available published data is low. This review will stimulate readers to carry out well designed, larger population based trials, so as to validate its use in dermatology practice.

Spina bifida is a developmental anomaly characterized by defective closure of the bony encasement of the spinal cord through which the spinal cord and meninges may or may not protrude. We report a rare case of a very long faun tail, which was in the form of a 20 inch long tail originating from the lumbosacral area in a rhomboidal pattern, measuring 10 x 8 inches. The case is being reported for its rare presentation of a 20 inch long faun tail with underlying spina bifida occulta.

Background The Virtual Data Warehouse (VDW) was created as a mechanism for producing comparable data across sites for purposes of proposing and conducting research. The database is “virtual” in the sense that the data remain at the local sites; there is no multi-site physical database at a centralized center. At the core of the VDW are a series of standardized file definitions. Content areas and data elements that are commonly required for research studies are identified, and data dictionaries are created for each of the content areas, specifying a common format for each of the elements—variable name, label, description, code values, and value labels. Local site programmers have mapped the data elements from their HMO’s data systems into this standardized set of variable definitions, names, and codes, as well as onto standardized SAS file formats. This common structure of the VDW files enables a SAS analyst at one site to write one program to extract and/or analyze data at all participating sites.

Background/Aims SAS Programmers support their Virtual Data Warehouse (VDW) in many venues. These include collaboration and deliverables for multiple projects both internal and external. Such requests include ad-hoc, feasibility and grants proposal data requests from both internal and external investigators and researchers. Different VDW workgroups and VDW site programmers use different naming conventions and standards; this adds to the confusion and produces an unclean environment. SAS Programmers have to make changes to programs over time as the data requirements continually change and must be maintained and accurate per update. The aim of this paper is to suggest a unified method to ensure a cohesive culture amongst the VDW participants by standardized naming conventions. This paper also focuses on setting guidelines for VDW workgroup members and multi-site study programmers regarding creating documents, complying with standard templates, and ensuring guidelines.

Background/Aims This presentation will focus on data quality issues experienced by new HMO Research Network (HMORN) sites while building Virtual Data Warehouse (VDW) demographics, enrollment, utilization, and provider tables from scratch. Our goal is to benefit new sites joining the HMORN by providing a heads-up on anomalies to look for and what to expect of the initial data quality check.

Background/Aims Geocodes are used to link individual enrollee records to demographic information from the Census Bureau. Currently, many of the HMORN VDW sites are utilizing software such as MapMarker+ to geocode their data. Acquiring third-party software capable of street-level geocoding is an additional expense that new and current HMORN sites may not have to incur. Geocoding at the street level has been added to the SAS/GRAPH module in the third maintenance release of SAS 9.2, enabling users more flexibility to create powerful geographic analyses and data graphic presentation. This presentation will focus on creating the VDW CENSUS table using PROC GEOCODE in SAS/Graph.

Background Despite consistent recommendations in numerous guidelines sponsored by professional societies, screening youth for familial hypercholesterolemia (FH) and/or those with a family history of premature cardiovascular disease (CVD) identifies only a small percentage of high-risk youth. By linking parent and child data in the virtual data warehouse, we can assess current screening practices, factors that impact screening practices and ultimately strategies aimed at improving childhood screening.

Objectives Understanding the prevalence and outcomes of cardiovascular disease across different health systems will enable organizations to effectively use clinical datasets to monitor and improve the care delivered to their patients. Framed within the context of comparative effectiveness research, this study utilized comprehensive administrative datasets to describe outcomes of hospital readmission, Emergency Department (ED) use, and mortality following a cardiovascular event (myocardial infarct, congestive heart failure, angina, stroke). We examined patients within the same geographic region (central Texas) at Scott & White Healthcare (SWHP) and the Veterans Health Administration (VA).

Dyschromatosis universalis hereditaria is an infrequently occurring genodermatosis with peculiar pigmentary changes, consisting of varying sized, intermingled hyperpigmented and hypopigmented macules that give an overall impression of mottling. We hereby report a case of dyschromatosis universalis hereditaria in a young female with a family history of the disorder.

Dermatofibrosarcoma protuberans (DFSP) is a low-grade tumor with rare metastasis. A 26-year-old male presented with multiple cutaneous nodular lesions of DFSP since 3 months along with distant metastasis to the brain, pleura, and muscles that were detected on investigations. The case is being reported due to its rare disseminated cutaneous with systemic metastasis.

Imatinib is a tyrosine kinase inhibitor approved as a first line treatment for chronic myeloid leukemia and gastrointestinal stromal tumors. Usually the drug is well-tolerated with hematological adverse effects being most commonly seen. Dermatological side effects are seen in 9.5-69% of patients on imatinib; majority of which are minor and self-limiting. We, hereby, report a case series of erythroderma occurring secondary to imatinib in two patients with chronic myeloid leukemia. Both the patients improved upon the discontinuation of the drug. The literature review revealed only six probable cases of erythroderma due to imatinib. So, this case series is being reported for the rarity of this adverse effect of imatinib.

Thirty patients with localised stable vitiligo were selected from the Out Patient Department for cosmetic tattooing. Of them, 19 cases (63.3%) had skin patches, 9 cases (30%) had mucosal patches, and 2 cases (6.7%) had both skin and mucosal involvement. After complete clinical evaluation, cosmetic tattooing was performed on these patients, and they were followed up for 6 months. As results, 23 cases (76.7%) had excellent color matching, 2 cases (6.7%) had good color matching, and 5 cases (16.6%) had pigment shedding. Excellent results were seen in all mucosal patches. Dark complexion cases showed better results than fair complexion ones.

Background/Aims Family relationship data in the Scott & White Virtual Data Warehouse (VDW) gathered from multiple sources across the institution is a rich resource that provides an opportunity to study patterns of inherited disease and the ability to evaluate the efficacy of targeted screening strategies. In an integrated healthcare delivery system, linkage of the parent and child (family) electronic health records (EHR) provides an opportunity to improve outcomes by implementing proactive/preventative screening and/ or treatment in offspring. Our study focuses on how linkage of the parent/ child EHR can be used to identifying youth at risk for a number of autosomal dominant inherited diseases.

Background/Aims This presentation will focus on challenges faced by new HMO Research Network (HMORN) sites and their experiences with the Virtual Data Warehouse (VDW) tables for version 3 specifications. The step-by-step procedure developed by Scott and White will be showcased to provide a head start for new incoming sites. Sharing lessons learned during our one year in the HMORN VDW, our objective is to provide best practices regarding resources, time allocation, priorities, schedules, financing, backups, and possible available alternatives.