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Phenotyping Software In USA
39 software items found
by:Seven Bridges Genomics based inCharlestown, MASSACHUSETTS (USA)
Across the world, numerous initiatives are currently underway to collect massive repositories of genomic and phenotypic data. These data have the potential to reveal transformative insights into the underpinnings of disease, novel therapeutic approaches, and in silico disease models. Seven Bridges ARIATM offers researchers a centralized solution for high throughput molecular and ...
by:Frameshift Labs, Inc. based inBoston, MASSACHUSETTS (USA)
The engine behind Mosaic. A population-scale variant warehouse enabling complex annotation, phenotype, and genotype queries in ...
by:AiCure based inNew York City, NEW YORK (USA)
Our hope is that it encourages researchers to use objective quantification of behavior in their analyses and through individual contributions becomes a central repository of novel methods in digital ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Next-generation sequencing (NGS) of the human exome has the potential to identify pathogenic variants responsible for complex phenotypes associated with rare ...
Manufactured by:Moberg Research, Inc based inAmbler, PENNSYLVANIA (USA)
Simplify analysis with the CNS Multimodal Database. Perform complex queries on a comprehensive database of physiological and phenotypic patient data. ...
Manufactured by:LemnaTec GmbH - Nynomic Group based inAachen, GERMANY
LemnaGrid is the image analysis component developed by LemnaTec to address these specific needs in phenotyping. The image analysis is graphically represented as a process chain and can be subsequently saved as a LemnaTec image analysis Grid. Each Grid is constructed of Grid Devices, where a device is the graphical representation of an algorithm, e.g. loading an image from the ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
Pave the way to smarter breeding by unraveling the causation elements in your population genomics. Quickly discover the phenotype-genotype correlations in any organism with NRGene’s complete trait-mapping package. We’ll generate a high-resolution recombination map which is used to reveal the complete segregation pattern in each progeny. Our special ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Over the last decade, substantial progress has been made in the discovery of genetic variants influencing a range of metabolic diseases.1 The advances in next generation sequencing (NGS) technologies have contributed to elucidation of the pathogenic role of variants associated with metabolic phenotypes, leading to a significant improvement in the throughput and diagnostic rate. ...
by:Indica Labs Inc. based inAlbuquerque, NEW MEXICO (USA)
HALO AI classifiers can be trained to quantify tissue classes, to segment tissue classes for analysis with other HALO image analysis modules, to find rare events or cells in tissues, and to categorize cell populations into specific ...
by:BC Platforms based inZürich, SWITZERLAND
BC | INSIGHT is a data and research management solution for clinical genomics studies. Genomic and phenotypic data is collected and stored on the platform, and users have access to data and tools through an application account. All common data types for NGS, GWAS, variant analysis, linkage, and other statistics can be managed on the platform. ...
by:Ovation based inPortland, MAINE (USA)
Also included is a Differential Gene Expression (DGE) analysis comparing gene expression on diseased and normal tissue from the same patients. *This sample dataset comes pre-packaged with WGS & RNAseq data linked to phenotypic data sourced by Ovation to provide an example turnkey solution. Although this dataset is linked using Datavant tokenization, it can be linked to almost ...
by:Indica Labs Inc. based inAlbuquerque, NEW MEXICO (USA)
Indica Labs’ Highplex FL module allows for simultaneous analysis of an unlimited number of fluorescent markers in any cellular compartment – nucleus, cytoplasm, and/or membrane. With the option to define specific cell phenotypes according to marker positivity, this module is ideally suited for applications in immuno-oncology where multiple markers are required to ...
Manufactured by:PerkinElmer, Inc. based inShelton, CONNECTICUT (USA)
Quickly process, analyze, share, and store the vast volumes of data generated by high-content screening and cellular imaging, including 3D imaging, phenotypic screening, and cell painting – so you can get your answers sooner. Reduce time to results from days and weeks to ...
by:Paige AI, Inc. based inNew York City, NEW YORK (USA)
Using proprietary computational pathology with exclusive clinical data cohorts, Paige rapidly uncovers and validates phenotypic patterns that are not identifiable using existing methodologies and deploys the AI globally. ...
by:nference, Inc. based inCambridge, MASSACHUSETTS (USA)
Our scientists use the nference platform and data in collaboration with your teams to tackle your most important questions and challenges. nference is creating the largest labeled EMR dataset in healthcare. EMR data contains longitudinal real-world, “deep data” rich in clinical phenotypes and outcomes spanning across therapeutic areas, but exists in in largely ...
by:TeselaGen Biotechnology, Inc. based inPortola Valley, CALIFORNIA (USA)
With the DISCOVER module, teams can combine their knowledge and data with AI algorithms built to understand biology — leading to new, high performance bio based products faster than ever before. Our AI models allow you to converge on an optimal product ten times faster than using traditional approaches. ...
by:Advaita Bioinformatics based inAnn Arbor, MICHIGAN (USA)
iVariantguide allows you to quickly analyze and interpret your VCF file with publication-ready visualizations. Single sample, Tumor/Normal, Pedigree, and Group v. ...
by:Karyosoft Inc. based inCarmel, INDIANA (USA)
Easy to use with just a few clicks and web-based. Flexibility to use single or multiple samples. 41 to 168 days saving for 96 samples. A simple report for whole-genome variant distribution. All your genomic variants information at your ...
by:Frameshift Labs, Inc. based inBoston, MASSACHUSETTS (USA)
Mosaic is a collaborative platform for organizing, visualizing, and understanding genomic ...
Manufactured by:Cell Microsystems based inDurham, NORTH CAROLINA (USA)
The CellRaft® Technology is powered by our innovative software that controls the automated imaging and CellRaft isolation functions of the platform. Most importantly, the CellRaft Cytometry™ feature allows for software-driven decision-making to identify CellRafts of interest. User-defined attributes ranging from cell shape to colony size to fluorescence intensity allow for precise ...