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Gene Mutation And Expression Software
13 software items found
Manufactured by:Alithea Genomics based inEpalinges, SWITZERLAND
Demultiplexing, alignment and gene counts at the click of a ...
by:Champions Oncology, Inc. based inHackensack, NEW JERSEY (USA)
Model Select® is Champions' online, searchable database that contains essential data on our PDX tumor models. We have enhanced details on the molecular features of our models, including gene mutations identified through Whole Exome Sequencing (WES) and gene expression levels quantified using RNASeq technology, making Model ...
by:Champions Oncology, Inc. based inHackensack, NEW JERSEY (USA)
Cell Line Select® is Champions' online, searchable database containing over 100 Human cancer cell lines, including characterization datasets such as gene mutations identified through Whole Exome Sequencing (WES) and gene expression levels quantified using RNASeq technology. ...
by:Qlucore AB based inLund, SWEDEN
Ongoing work to comply with the CE-IVDR (clinical use). The program includes classifier models and supportive gene fusion analysis. Qlucore Diagnostics is a scalable diagnostic solution from data to report, improving clinical? workflow? with easy-to-understand analysis and visualization? for better communication between lab, clinicians, and ...
by:SoftGenetics, LLC. based inState College, PENNSYLVANIA (USA)
NextGENe software is the perfect analytical partner for the analysis of desktop sequencing data produced by Illumina® iSeq, Miniseq, MiSeq, NextSeq, HiSeq, and NovaSeq systems, Ion Torrent Ion GeneStudio S5, PGM, and Proton systems as well as other platforms. NextGENe software runs on a Windows® Operating System, which provides a biologist-friendly ‘point & click’ ...
by:Qlucore AB based inLund, SWEDEN
Qlucore's clinical diagnostics solutions for multi-omics companion and precision diagnostics include AI-powered, disease-specific machine learning based classifier models and are combined with patient-friendly visualizations in a an easy-to-use and cost-effective software solution which integrates with a wide range of data generating techniques and instruments. ...
by:Noldus Information Technology bv based inWageningen, NETHERLANDS
The Observer XT is the ideal tool for many researchers because it saves you time scoring behaviors and it allows you to synchronize and analyze multiple signals (video, audio, physiology, etc) all ...
by:Agronomix Software Inc. based inWinnipeg, MANITOBA (CANADA)
Develop hybrids and varieties faster, more efficiently and with greater precision via bioinformatics tools integrated into your breeding ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Most rare and inherited diseases have a neurological component, likely because more than 80% of human genes are expressed in the brain.1 Neurological disorders are multifactorial and heterogeneous, meaning that their genetic basis is often poorly understood. Indeed, only 30-50% of neurological disorders have a molecular genetic diagnosis.2 ...
by:nference, Inc. based inCambridge, MASSACHUSETTS (USA)
We offer a vertically integrated, end-to-end solutions and software to make the most of your data. Maximizing your data to improve patient outcomes. We partner with you to securely process and transform your raw unstructured and semi-structured EMR data into structured data that can be used to develop solutions to healthcare’s biggest ...
by:Igenbio, Inc. based inChicago, ILLINOIS (USA)
ERGO 2.0 provides a systems biology informatics toolkit centered on comparative genomics to capture, query, and visualize sequenced genomes. Using Igenbio's proprietary algorithms, and the most comprehensive genomic database integrated with the largest collection of microbial metabolic and non-metabolic pathways, ERGO™ assigns functions to genes, integrates genes into pathways, and ...
by:Ovation based inPortland, MAINE (USA)
This Ovation IBD Genomic and Clinical Linked Data sample dataset is a packaged, real-world observational cohort of 10 Inflammatory Bowel Disease (IBD) subjects. It's available at no cost for scientists interested in evaluating Ovation’s Whole Genome Sequencing and RNAseq data with up to 30x coverage. The data is linked with clinical data, including full redacted pathology reports, ...
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 semi-structured and ...