Cohort research inside your data rules.
From scattered to one record.
Today
- Cohort analysis under strict ethics and data rules.
- Analysis code and notes are hard to trace later.
- Writing takes time away from the lab and the clinic.
With Cytogent
- Work stays inside the project and its permissions.
- Each step is logged with its inputs and sources.
- Papers and reports drafted from cited results.
Files and tools scattered today · one project with its agents
The workflows your team uses.
Literature & evidence
Papers, patents, protocols and registries in one query. Every claim points to its source.
See this workflowClinical trials, full cycle
Protocol drafts, site feasibility, cohort criteria, CRFs, statistical analysis plans, monitoring summaries and CSR drafts.
See this workflowCRISPR & genome editing
Guide design, off-target review and screen analysis, documented for the lab.
See this workflowProtein studies & design
Structure prediction, binding analysis and sequence design, with validation reports.
See this workflowOne project, step by step.
- 01
A cohort question is approved
The study has its question and its ethics approval.
- 02
Data is attached
The cohort data goes into a project only the team can see.
- 03
The analysis runs
Step by step, each one logged with its inputs.
- 04
The paper is drafted
Results and methods, with every claim cited.
Each stage has its owner · the record fills in as it passes
Inside your data rules.
Access by request only
No self sign-up. Every account is reviewed.
DoneRole-based access
Owner, editor and viewer roles per project.
DoneA research tool
Not a medical device. It makes no clinical decisions.
StatementBring your next question.
Tell us your field and what you want to do. We set up the workspace around it.
Request access