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Genomics Software In Asia Middle East
13 software items found
by:ArrayGen Technologies based inPune, INDIA
The ANG genome browser is a visualization tool, developed by ArrayGen Technologies Pvt. Ltd. This is a fast and an efficient genome browser, built with Javafx and Java swing. ANG Genome Browser was built for latest next generation sequencing data analysis. ...
by:Phenome Networks based inRehovot, ISRAEL
Phenome One’s revolutionary Genomics module (a.k.a. Unity) uses advanced GWAS and QTL analysis and standardized terminology to identify the genetic markers affecting the traits you are looking for. The Genomics module allows you to see the big picture, by evaluating marker effects on phenotypes not only in your study but also in different experiments and ...
by:inDNA Research Labs based in, INDIA
OncoNGx Genomic Workbench is a HIPAA compliant cloud based informatics and clinical annotation platform that will translate sequence (NGS) data from a Cancer diagnostic gene panel into actionable report/information for ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
Receive the highest genome assembly quality in a record time. DeNovoMAGIC™ has already been successfully used by hundreds of customers around the globe, building the most challenging reference genomes. Now, with the availability of an accurate long read data our quality got even better. The newest version of DenovoMAGIC™ employs a real hybrid assembly ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
Get a jump start on your breeding program even before the greenhouses are up! Identify your desired traits and create your breeding plan in silico with our ready-to-use genomics ...
by:Partek Incorporated based inChesterfield, MISSOURI (USA)
Partek® Genomics Suite® is a statistical analysis software that lets you analyze microarray, qPCR, and pre-processed NGS data right from your desktop computer. It is fast, agile, and memory efficient. With a user-friendly interface, rich visualizations, and guided workflows for common genomics assays, Partek Genomics Suite gives ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
All-to-all linear mapping of multiple denovo assemblies enables intra-species gene content variation exploration. A high-quality reference genome is a great starting point, yet in many plant species the genomic diversity within the species can be as high as 50% of the genomic sequence. The discovery of genomic variations ...
by:Partek Incorporated based inChesterfield, MISSOURI (USA)
You can calculate pathway enrichment, detect disrupted or influential pathways, search for specific pathways and genes, and color code genes based on their p-values and fold changes. Partek Pathway integrates inside Partek Flow or Partek Genomics Suite ...
by:EvidNet Inc. based inSeongnam-si, SOUTH KOREA
Based on our experience working with structured and unstructured hospital EMR data, we can convert, expand, extend, and integrate data from various sources including national claims data (HIRA/NHIS), national statistics data (Statistics Korea), medical imaging data, genomic data and patient generated health data ...
by:Portable Medical Technology Ltd. based inKillarney, IRELAND
ONCOassist is the go-to app for oncology and haematology professionals. It offers easy access to relevant, up-to-date tools and content when and where it is needed. With the advent of genomic sequencing, combined with an aging population, and new therapies. The decision-making process for oncology/haematology HCP’s is becoming increasingly complex. Unfortunately, there is ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
With Explore Cohort, review the prevalence of diagnoses, treatments, and procedures among your cohort, retrieve lab value means and standard deviations, and count instances of variants by genome. Use Criteria Analysis to rank order your query criteria by the number of patients they disqualify. Rate of Arrival predicts the volume of new patients who will meet your criteria in the ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
Data sourced from the EHRs of U.S. healthcare organizations forms the foundation of this combined data asset, providing a rich clinical picture of patients from encounters with providers, lab results, procedures, medication orders, and genomics. Medical and pharmacy claims provide insight into a patient’s care before and after these encounters, regardless of provider. ...
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 ...