ArcGIS
ArcGIS is a geographic information system (GIS) for working with maps and geographic information. The license is valid until September 1st each year.
ArcGIS is a geographic information system (GIS) for working with maps and geographic information. The license is valid until September 1st each year.
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. Bioconductor uses the R statistical programming language, and is open source and open development. It has two releases each year, 1296 software packages, and an active user community.
"BioCyc.org is a microbial genome Web portal that combines thousands of genomes with additional information inferred by computer programs, imported from other databases and curated from the biomedical literature by biologist curators. BioCyc also provides an extensive range of query tools, visualization services and analysis software." (Karp et al., 2019)
Biorender is an online graphics tool for building high quality figures for the life sciences. Our institutional account will allow discounted access to all faculty, staff and students. All licenses expire on May 30th of each year regardless of when the license is purchased.
CLC Genomics Workbench allows users to analyze and visualize nexg generation sequencing (NGS) data. CLC Genomics Workbench supports the complete resequencing pipeline for detecting and comparing genetic variants.
Cytoscape is an open source software platform for visualizing molecular interaction networks and biological pathways and integrating these networks with annotations, gene expression profiles and other state data.
Estimate variance-mean dependence in count data from high-throughput sequencing assays and test for differential expression based on a model using the negative binomial distribution. Available through the bioconductor package in R
Endnote is a bibliographic management tool for storing and accessing shared references, documents and files. Endnote allows the autmated insertion of citations in MS Word in over 6000 styles. Endnote can retrieve the full text of all articles in your library from freely available sources and the Samuel J. Wood library's subscriptions.
FCS Express analyzes raw flow cytometry data and allows production of presentations, spreadsheets and reports.
The FlowJo workspace is a powerful statistical environment that is used for immunophenotyping, cell cycle, proliferation, kinetics studies, quantitative population comparison, or plate screening assays.
Annual license cost is determined by the number of active users each quarter. Thus we can only provide an estimate of the cost based on current usage.
GraphPad Prism combines scientific graphing, comprehensive curve fitting (nonlinear regression), understandable statistics, and data organization. While it won't replace a heavy-duty statistics program, Prism lets you easily perform basic statistical tests commonly used by laboratory and clinical researchers. Prism offers t tests, nonparametric comparisons, one-, two- and three-way ANOVA, analysis of contingency tables, and survival analysis. Analysis choices are presented in clear language that avoids unnecessary statistical jargon.
i2b2 enables researchers to discover cohorts of patients using data from EHR systems. Through a point-and-click interface, researchers can build queries drawing from demographics, diagnoses, procedures, medications, and results recorded in Epic, the EHR system of Weill Cornell Physician Organization outpatient clinics (access to data from Eclipsys/Allscripts Sunrise Clinical Manager, the EHR system of NewYork-Presbyterian inpatient units, is planned). i2b2 supports different types of queries of clinical data, including whether clinical concepts occurred at any point in a patient’s medical
LabArchives is a secure, cloud-based electronic lab notebook (ELN) designed for research. This ELN system enables researchers to capture, manage, store, and share information and data. LabArchives facilitates collaboration amongst researchers within a loab, institution, and with external stakeholders.
DNASTAR's Lasergene Molecular Biology Suite is our comprehensive package of molecular biology software, meeting all of your sequence analysis needs. Supported workflows include performing multiple and pairwise sequence alignments, identifying genes, assembling contigs of Sanger sequences, creating virtual clones, designing primers, and more.
Ledidi Core is a secure web-based platform for research projects and clinical registries with functionality for study design, creation of data entry forms and eCRFs in combination with built-in-tools for statistical analysis and data visualization. The statistical analyses include descriptive statistics, parametric and non-parametric tests, regression analyses, contingency tables and survival analyses. It is suited for international collaborations, or for single or multi-center projects.
MacVector provides numerous functions for DNA and protein analysis, including sequence editing, primer design, internet database searching, protein analysis, multiple sequence alignment, phylogenetic reconstruction, coding region analysis, and agarose gel simulation.
The MATLAB platform is optimized for solving engineering and scientific problems. The matrix-based MATLAB language is the world’s most natural way to express computational mathematics. Built-in graphics make it easy to visualize and gain insights from data. A vast library of prebuilt toolboxes lets you get started right away with algorithms essential to your domain. The desktop environment invites experimentation, exploration, and discovery. These MATLAB tools and capabilities are all rigorously tested and designed to work together.
Medicare is the federally funded program that provides health insurance for the elderly, persons with end-stage renal disease, and some disabled. For persons age 65 and over, 97 percent are eligible for Medicare. Almost all Medicare beneficiaries have Part A coverage that includes hospital, skilled-nursing facility, hospice and some home health care. Information about Medicare eligibility and enrollment is available for all persons included in the SEER-Medicare data (both cancer and non-cancer cases). Medicare claims (bills) are available only for persons with fee-for-service coverage.
Microsoft Access is a database management system (DBMS) from Microsoft that combines the relational Microsoft Jet Database Engine with a graphical user interface and software-development tools. MS Access is freely available for WCM ITS-tagged PCs through the Software Center application.
The National Health and Nutrition Examination Survey (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The survey combines interviews and physical examinations. NHANES is a major program of the National Center for Health Statistics (NCHS), which is part of the Centers for Disease Control and Prevention (CDC).
The New York City Clinical Data Research Network (NYC-CDRN) has been established to improve and streamline research in an effort to advance patient-centered research. NYC-CDRN uses a large volume of robust, high-quality patient data and support services from a collaboration of more than 20 partners, including WCM and NYP. The NYC-CDRN collects comprehensive medical histories for what will be as many as 6 million patients.
Qualtrics is web based software that allows the user to create surveys and generate reports without having any previous programming knowledge. Qualtrics enables you to do surveys, feedback and polls using a variety of distribution means. Results can be viewed in reports and can be downloaded. Qualtrics allows you to share surveys and results as well as collaborating with other users.
R is a free software environment for statistical computing and graphics. It compiles and runs on a wide variety of UNIX platforms, Windows and MacOS.
RStudio is an integrated development environment (IDE) for R. It includes a console, syntax-highlighting editor that supports direct code execution, as well as tools for plotting, history, debugging and workspace management.
REDCap is a PHP-based system, developed by Vanderbilt University and currently managed and updated through a national consortium, that supports the rapid setup of secure, Web-based study-specific database systems and associated forms. It provides full field validation capabilities (customized to each study), import/export (including export to common statistical packages such as SAS, SPSS and Excel), and file upload/management functions.
SAP Lumira (formerly called SAP Visual Intelligence) is a self-service, data visualization application for business users.
SAS (Statistical Analysis System) is a software suite developed by SAS Institute for advanced analytics, multivariate analyses, business intelligence, data management, and predictive analytics. The suite purchased through WCM includes
The SAS license is valid from May 15, 2021 to May 14, 2022
The SEER*Stat statistical software provides a convenient, intuitive mechanism for the analysis of SEER and other cancer-related databases. It is a powerful PC tool to view individual cancer records and to produce statistics for studying the impact of cancer on a population. SEER*Stat software is distributed with the SEER Research Data and you must have access to the data before using the software.
The SEER-Medicare data reflect the linkage of two large population-based sources of data that provide detailed information about Medicare beneficiaries with cancer. The data come from the Surveillance, Epidemiology and End Results (SEER)External Web Site Policy program of cancer registries that collect clinical, demographic and cause of death information for persons with cancer and the Medicare claims for covered health care services from the time of a person's Medicare eligibility until death.
The Limited Access DMF (DMF) from the Social Security Administration (SSA) contains over 86 million records created from SSA payment records. This file includes the following information on each decedent, if the data are available to the SSA: social security number, name, date of birth, date of death. The SSA does not have a death record for all persons; therefore, SSA does not guarantee the veracity of the file. Thus, the absence of a particular person is not proof this person is alive. SSDMF database is updated once a week.
IBM SPSS Statistics is an integrated family of products that helps to address the entire analytical process, from planning and data collection to analysis, reporting and deployment. With more than a dozen fully integrated modules to choose from, you can find the specialized capabilities you need to increase revenue, outperform competitors and make better decisions.
Stat/Transfer is designed to simplify the transfer of statistical data between different programs. Stat/Transfer will automatically read statistical data in the internal format of one of the supported programs and will then transfer as much of the information as is present and appropriate to the internal format of another. Stat/Transfer preserves all of the precision in your data, while automatically minimizing the size of your output data set. Stat/Transfer also allows control over the storage format of your output variables.
Stata is a complete, integrated statistical software package.
SPARCS is a comprehensive all payer data reporting system, initially created to collect information on discharges from hospitals. SPARCS currently collects patient level detail on patient characteristics, diagnoses and treatments, services, and charges for each hospital inpatient stay and outpatient (ambulatory surgery, emergency department, and outpatient services) visit; and each ambulatory surgery and outpatient services visit to a hospital extension clinic and diagnostic and treatment center licensed to provide ambulatory surgery services.
The Surveillance, Epidemiology, and End Results (SEER) Program of the National Cancer Institute provides information on cancer statistics. The SEER research data include SEER incidence and population data associated by age, sex, race, year of diagnosis, and geographic areas (including SEER registry and county). SEER research data are released every Spring based on the previous November’s submission of data. Additional datasets are available including: Standard Population Data, U.S. Mortality Data, and U.S. Population Data.
TRANSFAC provides data on eukaryotic transcription factors, their experimentally-proven binding sites, consensus binding sequences (positional weight matrices) and regulated genes. TRANSCompel contains data on eukaryotic transcription factors experimentally proven to act together in a synergistic or antagonistic manner.