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Average Ratings 0 Ratings
Description
2bPrecise offers revolutionary point-of-care solutions that form the basis for achieving success in scalable precision medicine. Are patients not responding as expected to initial treatments for prevalent conditions? Utilizing pharmacogenomics allows for the identification of medications that are not only safer but also more effective for individuals. Immediate access to test results significantly reduces the reliance on “trial-and-error” prescribing methods, thereby speeding up patient recovery. Comprehensive data-gathering tools focused on genetics assist in identifying and revealing potential risks. The integration of in-workflow Pedigree visualization enables healthcare providers to pinpoint individuals who may benefit from genetic testing, guiding them towards the most effective treatment options. When faced with complex diagnostic challenges, such as symptoms like seizures or syncope that may align with various conditions, germline tests can identify hereditary traits that aid in making accurate diagnoses. Having access to relevant and actionable results during the clinical decision-making process empowers healthcare professionals to take proactive steps in patient care. Ultimately, these advancements pave the way for a more personalized and effective healthcare experience.
Description
Genome Computer allows you to transform your genetic information into a downloadable, AI-compatible .genome bundle that you can store, self-host, and analyze using tools like Genome Intelligence, Codex, Claude Code, Cursor, or others that are compatible. This open format reorganizes the standard data typically found in a VCF into a structured and queryable bundle, with variants neatly arranged in swift columnar tables alongside trait associations, facilitating research and providing insights into gene-level context, polygenic scores, pharmacogenomics, and clear data lineage. Orders for whole-genome sequencing are derived from gVCF data, ensuring that both identified variants and confidently sequenced regions where no variants exist are preserved, with FASTQ files available upon request. Additionally, VCF or TXT files from other providers can be seamlessly converted, imputed where necessary, annotated, scored, and prepared for AI analysis. With Genome Intelligence, users can pose questions based on their specific genetic information, juxtapose new research with their genotypes, and delve deeper into the field of genetics, ultimately enriching their understanding of personal health and ancestry. This capability empowers individuals to take control of their genetic data and engage with it in ways previously not possible.
API Access
Has API
No
API Access
Has API
Yes
Integrations
Claude Code
No
Cursor
No
OpenAI Codex
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
$15 per month
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
No
Vendor Details
Company Name
2bPrecise
Founded
2016
Country
United States
Website
2bprecisehealth.com
Vendor Details
Company Name
Genome Computer
Country
United States
Website
genome.computer/
Product Features
Patient Case Management
Activity Tracking
No
Assessment Notes
No
Billing & Invoicing
No
Calendar Management
No
Candidate Identification
No
Case List Management
No
Eligibility Verification
No
HIPAA Compliant
No
Medical History Records
No
Patient Records
No
Referral Management
No
Treatment Planning
No