- Home
- Software
- asia middle east
- genomics redefines the boundaries of fungal genomics
Refine by
Locations
- Asia & Middle East
- Afghanistan
- Armenia
- Azerbaijan
- Bahrain
- Bangladesh
- Bhutan
- Brunei Darussalam
- Cambodia
- China
- East Timor
- Georgia
- Guam
- Hong Kong
- India
- Indonesia
- Iran
- Iraq
- Israel
- Japan
- Jordan
- Kazakhstan
- Kuwait
- Kyrgyzstan
- Laos
- Lebanon
- Malaysia
- Maldives
- Mongolia
- Myanmar
- Nepal
- North Korea
- Oman
- Pakistan
- Palestinian Territories
- Philippines
- Qatar
- Russia
- Saudi Arabia
- Singapore
- South Korea
- Sri Lanka
- Syria
- Taiwan
- Tajikistan
- Thailand
- Turkmenistan
- United Arab Emirates
- Uzbekistan
- Vietnam
- Yemen
Applications
- Bioinformatics software solutions for single cell rna-seq sector
- Bioinformatics software solutions for gene expression sector
- Bioinformatics software solutions for variant detection sector
- Bioinformatics software solutions for CNV analysis sector
- Bioinformatics software solutions for metagenomics sector
- Genomic Workbench Software for Cancer Biology
Genomics Redefines The Boundaries Of Fungal Genomics Software In Asia Middle East
16 software items found
by:Partek Incorporated based inChesterfield, MISSOURI (USA)
Partek® Pathway™ allows you to explore complex biological relationships and pathways between genes to discover meaningful biological insights. 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 ...
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 to benefit the data quality and ...
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. It is platform independent and much simpler to ...
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 population ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
The full set of base analytics are enabled on every network, except for anonymous networks such as Linked, where HCO attribution is not shown. 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 ...
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 not always easy ...
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 biologists, bioinformaticists, and statisticians a single, ...
Manufactured by:Agilent Technologies, Inc. based inSanta Clara, CALIFORNIA (USA)
Agilent's GeneSpring provides powerful, accessible statistical tools for intuitive data analysis and visualization. Designed specifically for the needs of biologists, GeneSpring offers an interactive environment that promotes investigation and enables understanding of Transcriptomics, Metabolomics, Proteomics and NGS data within a biological context. GeneSpring allows you to quickly and reliably ...
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 is a hot scientific subject in many research papers, but current ...
by:EvidNet Inc. based inSeongnam-si, SOUTH KOREA
EVIX-MART™ is an on-demand ETL and data quality management service. 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: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: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. Pre-existing ...
by:Insilico Medicine based inPak Shek Kok, HONG KONG
A roadmap to successful disease research and target identification strategies requires considerable resources spent on search, collection and interpretation of data during several months of work. PandaOmics provides a unique opportunity to both explore the unknown of OMICs data and interpret it in the context of all the scientific data generated by the scientific ...
by:LabOS based inTikva, ISRAEL
LabOS Genetics empowers labs with cutting-edge tools for genetic and genomic testing, delivering real-time, accurate results that enable confident decision-making to improve patient ...
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: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 ...