Emedgene
Illumina Connected Software
  • Get Started with Emedgene
    • Get started with Emedgene
    • How can Emedgene help you solve a case?
  • Emedgene analyze manual
    • Getting around the platform
      • Top navigation panel
      • Emedgene Applications menu
      • Dashboard
      • Settings
      • User roles
      • Help
      • Okta identity management
    • Managing data storage
      • Manage data storages
      • Manage Azure Blob data storage
      • Manage S3 credentials
      • Manage BaseSpace storage
      • Manage GCS storage (V37.0+)
      • Bring Your Own Bucket
      • Bring Your Own Key
    • Cases tab
      • Cases tab
      • Cases table
      • Case status
      • Browse and select cases
      • Case details
    • Creating a single case
      • Add a new case
      • Select sample type
      • Create a family tree
      • Family tree legend
      • Add a sample
      • Supported Variant callers
      • Adding patient info for the proband
      • Adding patient info for the non-proband samples
      • Secondary findings
      • Labeling a case
      • Gene list
      • Supported parental ethnicities
    • Creating multiple cases
      • Batch case upload from platform
      • CSV format requirements
      • Batch case upload via CLI
    • Reviewing a case
      • Individual case page
      • Individual case page: Top bar
      • Individual case page: Top bar
      • Candidates tab
      • Most Likely Candidates and Candidates
      • Genome Overview
      • Analysis tools tab
      • Variant table columns
      • Variant table
      • Variant search
      • Multiselection of variants and bulk actions (34.0+)
      • Download variants
      • Manually add variants to a delivered case
      • Filters/Presets panel
      • Filters
      • Presets
      • Preset groups
      • Variant Type Filters
      • Variant Effect Filters
      • Quality Filters
      • Polymorphism Filters
      • Gene Filters
      • Phenomatch Filters
      • Inheritance Filters
      • Zygosity Filters
      • User Filters
      • Evidence page
      • Phenotypic match strength
      • Lab tab
      • Versions tab
      • Editing an existing case
      • Finalizing a case
      • Clinical Report
      • Reflex genetic testing
      • Variant zygosity notations
      • STR calling and interpretation
    • Variant page
      • Variant page
      • Variant page top bar
      • Variant tagging widget
      • Variant activity panel
      • Desktop apps panel
      • Clinical Significance section
      • Summary section
      • Quality section
      • Visualization section
      • Population Statistics section
      • Related Cases section
      • CNV overlap percentage
      • Evidence section
      • ACMG SNV Classification wizard
      • Logic behind ACMG classification of SNVs
      • ACMG CNV Classification wizard
      • Variant page sidebar (2.29+)
    • Variant visualization setup
      • Enabling visualization for a VCF case
      • Integration between emedgene and desktop IGV
      • Loading alignment files to your desktop IGV (32.0+)
    • Analyze Network
      • Analyze Network Setup
      • Network sharing configuration
      • Case subject consent for extended sharing
      • Public vs Private network
      • Create a network
      • Set network data sharing policy
      • Leave a network
      • Delete a network
    • Settings
      • My settings
      • Management
      • User Management
      • Network
      • Organization Settings (33.0+)
        • Quality parameters (38.0+)
    • Integrations
      • Automatic Case Creation from ICA - Cyto Array Analysis
      • API Beginner Guide
      • Advanced API Implementations
      • API Key Generation
      • BSSH Integration
      • ICA Integration
      • Webhook Integration
  • Emedgene Curate Manual
    • Curate overview
      • Curate overview
      • Emedgene Applications menu
      • Curate navigation panel
      • Genome assemblies supported by Curate
    • Curate Variants
      • Curate Variants overview
      • Curate Variant table
      • Curate Variant page
      • How to add a variant to Curate
      • Curate Variant annotations in the case
    • Curate Genes (2.28+)
      • Curate Genes overview
      • Curate Gene table
      • Curate Gene page
      • How to add a gene to Curate
    • Import Curate annotations to the case (30.0+)
      • Import Curate Variant annotations to the case (30.0+)
      • Import Curate Gene annotations to the case (30.0+)
  • Integrations
    • API Beginner Guide
  • Frequently Asked Questions
    • All FAQ
      • Which browser should I use with Emedgene?
      • Emedgene annotations and update frequency
      • How do I use developer tools to collect logs?
      • Can I analyze Illumina Complete Long Reads in Emedgene?
      • How do I prepare VCF files generated by DRAGEN MANTA to be used as input for Emedgene?
      • Source of gnomAD data for small variants on GRCh38
      • How are MNVs handled on the platform?
      • Support for gene lists with up to 10,000 genes
      • Genomic Regions by Case Type
      • How do I analyze mtDNA variants?
      • Can I use exome data for CNV detection?
      • How does joint calling work on Emedgene?
      • What is the required format for a BED file defining a kit?
      • Which reference genomes can I use?
      • How do I move between organizations?
      • How do I check the version of my environment?
      • "Failed to generate report". What should I do?
      • How do I prepare VCF files generated by Dragen STR (ExpansionHunter) to be used as input?
      • How does Emedgene Analyze prioritize transcripts?
      • How does Emedgene Analyze merge variants from different sources?
      • Performance issue troubleshooting
      • How does Emedgene calculate variant effect and severity ?
      • How to I prepare metrics files generated by DRAGEN to be used as input for Emedgene
      • How are timekeeping and log timestamps kept accurate and consistent?
  • Release Notes
    • Workbench & Pipeline Updates
      • New in Emedgene V38.0 (June 3rd, 2025)
      • New in Emedgene V37.0 (February 20, 2025)
        • V37 Patches
      • New in Emedgene V36.0 (October 8 2024)
        • V36 Patches
      • New in Emedgene V35.0 (May 22nd 2024)
        • V35 Patches
      • New in Emedgene V34.0 (January 28th 2024)
        • V34 Patches
      • More release notes
        • New in Emedgene V33.0 (September 6th 2023)
          • V33 Patches
        • New in Emedgene V32.0 (June 8th 2023)
          • New pipeline 32 (June 8th 2023)
          • V32 Patches
        • New in emedgene 31 (March 1st 2023)
        • New in emedgene 30 (January 8th 2023)
        • New in emedgene 2.29 (August 25 2022)
        • New pipeline 5.29 (May 1st 2022)
        • New in emedgene 2.28 (May 1 2022)
        • New in emedgene 2.27 (March 7, 2022)
        • New in emedgene 2.26 (Dec 14, 2021)
        • New in emedgene 2.24-2.25 (Aug 11, 2021)
        • New in emedgene 2.23 (Jun 15, 2021)
        • New in emedgene 2.19-2.22 (Apr 8, 2021)
        • New in emedgene 2.16-2.19 (Dec 7, 2020)
        • New in emedgene 2.12-2.16 (Oct 18, 2020)
    • Knowledgebase Updates
      • 2025
        • Variant Databases (March 30th 2025)
        • Zoidberg 77 (March 17th 2025)
        • Zoidberg 76 (February 3rd 2025)
        • Zoidberg 75 (January 6th 2025)
      • 2024
        • Variant Databases (December 8th 2024)
        • Zoidberg 74 (December 2nd 2024)
        • Zoidberg 73 (October 21th 2024)
        • Variant Databases (September 22nd 2024)
        • Zoidberg 72 (September 10th 2024)
        • Variant Databases (July 21st 2024)
        • Zoidberg 71 (July 24th 2024)
        • Zoidberg 70 (June 3rd 2024)
        • Zoidberg 69 (April 19th 2024)
        • Variant Databases (April 9th 2024)
        • Zoidberg 68 (March 18th 2024)
        • Variant Databases (February 5th 2024)
        • Zoidberg 67 (January 28th 2024)
        • Variant Databases (January 5th 2024)
      • 2023
        • Zoidberg 66 (December 24th 2023)
        • Variant Databases (December 3rd 2023)
        • Zoidberg 65 (November 21th 2023)
        • Variant Databases (November 5th 2023)
        • Zoidberg 64 (October 24th 2023)
        • Variant Databases (October 8th 2023)
        • Zoidberg 63 (September 18th 2023)
        • Variant Databases (September 5th 2023)
        • Zoidberg 62 (August 23th 2023)
        • Zoidberg 61 (August 16th 2023)
        • Variant Databases (August 6th 2023)
        • Zoidberg 60 (July 30th 2023)
        • Variant Databases (July 2nd 2023)
        • Zoidberg 59 (June 18th 2023)
        • Variant Databases (June 4th 2023)
          • Variant Databases (May 7th 2023)
        • Zoidberg 58 (May 21th 2023)
        • Zoidberg 57 (April 16th 2023)
        • Variant Databases (April 2nd 2023)
        • Zoidberg 56 (March 19th 2023)
        • Variant Databases (March 11th 2023)
        • Zoidberg 55 (February 19th 2023)
        • Zoidberg 54 (January 16th 2023)
    • Change log
      • Change log pipeline v34
      • Change log pipeline 31
      • Change log workbench 31
      • Change log pipeline 30
      • Change log workbench 30
      • Change log workbench 2.29
      • Change log pipeline 5.29
      • Change log workbench 2.28
  • Legal
    • Privacy, Security & Compliance
    • Release Policy
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  1. Emedgene analyze manual
  2. Getting around the platform

User roles

Emedgene users are defined by roles. In Illumina environments only, Roles and Permissions are now managed through IAM (previously via User Management in EMG Settings) . Access to the User Management tab (Users card) is disabled and redirects to the IAM application.

The available roles for Emedgene in IAM are described below:

Emedgene Role/IAM Scope
Description

Acmg Tags

Allow user to see ACMG Tags

Acmg Tags Edit

Allow user to edit ACMG classification

Add New Test

Allow user to add new test

Apidocs

Allow user to see api docs

Auto Analysis

Allow seeing auto analysis results

Candidate Compound With

Allow user to merge and split compound variants

Change Finalized Test Status

Allow user the user to unlock a finalized case

Check Preset

Allow user to mark case's presets as reviewed

Comment

Allow user to activity comment

Comment Delete

Allow user to delete comment

Create Custom Preset Group

Allow user to create Custom Preset Group

Create Report

Allow user to create report template

Create Variant

Allow user to create variant manually

Detailed Version

Allow user to see all services versions

Developer

Allow user to see developer settings

Download

Allow user to download files

Due Date

Allow user to edit due date

Edit Case Labels

Allow edit labels of a case

Edit Test

Allow user to edit test's info

Evidence

Allow seeing evidence page

Evidence Edit

Allow user to edit the evidence page

Evidence Generate

Allow user to generate intial evidence

Evidence Pathogenicity Edit

Allow user to edit evidence pathogenicity

Evidence Text Edit

Allow user to edit evidence text

Gene Lists Read Only

Allow user to show the gene lists

Gnomad Genome

Allow user to see GnomAD Genome

Kms

Allow user to view Curate

Kms Create Gene

Allow user to create a new gene in Curate

Kms Create Variant

Allow user to create new variant in Curate

Kms Delete Variant

Allow user to delete a variant from Curate

Kms Export

Allow user to export/update variants from Analyze to Curate

Kms Export Data

Allow user to export genes and variants data from Curate

Kms Import Network Variant

Allow user to import from network variants from Curate

Kms Update Acmg

Allow user to update variant ACMG tags in Curate

Kms Update Disease Id

Allow user to update variant disease ID in Curate

Kms Update Gene Interpretation

Allow user to update gene interpretation in Curate

Kms Update Gene Note

Allow user to update gene notes in Curate

Kms Update Gene Transcript Ref Sequence

Allow user to update a gene selected transcript in Curate

Kms Update Interpretation

Allow user to update variant interpretation in Curate

Kms Update Note

Allow user to update variant note in Curate

Kms Update Pathogenicity

Allow user to update variant pathogenicity in Curate

Kms Update Transcript

Allow user to update variant transcript in Curate

Load Bam Igv

Allow user to load BAM files to desktop IGV

Manage Auto Analysis Tier

Allow user to update AI Shortlist mode from Org settings page

Manage Case Default Page

Allow user to manage default Case page

Manage Case Identifier

Allow user to manage case identifier

Manage Case Participants

Allow user to add or remove case participants

Manage Column Order

Allow user to manage analysis column order setting

Manage Empty Trash

Allow user to empty cases from trash bin

Manage Gene List Visibility

Allow user to manage gene list visibility

Manage Gene Lists

Allow user to manage gene lists

Manage Kit Bed

Allow user to manage kits and bed uploads

Manage Labels

Allow user to manage labels

Manage Multiple Tags

Allow user to enable multiple tagging

Manage Organization Dbs

Allow user to manage organization databases

Manage Platform Version

Allow user to manage platform version

Manage Poc

Allow user to update POC from Org settings page

Manage Pon

Allow user to add or delete PONs

Manage Pipeline Versions

Allow user to update pipeline version from Org settings page

Manage Quality Parameters

Allow user to manage sample quality configurations

Manage Report Timestamp

Allow user to manage report timestamp

Manage S3 Credentials

Allow user to manage organization's s3 credentials

Manage Sv Annotation

Allow user to manage SV annotation thresholds

Manage Test Presets

Allow user to create presets from gene lists

Manage Url Pattern

Allow user to manage organization URL pattern

Manager

Organizational admin (manager) role

Manager Edit Variant Tags

Allow user to manage variants tag

Manager Support Access

Enable/disable support access in management

Network

Allow user to see available networks, request to join, etc.

Network Create

Allow user to creare new network

Network Manage

Allow user to manage network

Pheno Score Col

Allow user to see the Phenomatch score in the Analysis table

Phenomatcher

Allow user to filter by phenotipic match

Preset Create

Allow user to create presets from analyze and settings page

Preset Delete

Allow user to delete a preset from the list of available Filterset in a preset group

Preset Group Create

Allow user to create and edit a preset groups

Preset Group Default

Allow user to assign a default preset group

Preset Group Download

Allow user to download a legacy preset group JSON file

Preset Group Hide

Allow user to hide a preset group

Preset Group Revert

Allow user to revert a migrated preset group

Preset Group Upload

Allow user to upload a JSON file to the create new preset group

Preset Lock

Allow user to lock and unlock of a preset

Preset Manage

Allow user to view/edit a preset in JSON format

Re Analysis Filter

Allow user to see re analysis candidates

Re Upload Tab

Allow user to re-upload files

Render Template

Allow user to preview a report template

Report

Allow user to export a report

Report Preview

Allow user to preview report as draft

Sanger Edit

Allow user to edit Sanger

Storage Provider

Allow user to manage storage providers

Tag Variant

Allow user to tag a variant

Test Status

Allow user to change a test status

Test Status Move To Trash

Allow user to change test status to move to trash

Test Status To Finalized

Allow user to change case status to finalized

Transcript Edit

Allow user to change the default transcript for variants

Unknown Phenomatch

Allow user to use unknown phenomatch variant filter

Upload

Allow user to upload samples

User

Regular user role

User Management

Allow user to manage users

User Read

Allow user access to organization data

User Rerun Case

Allow user to re-run cases

Versions Tab

Allow user to access the Versions tab

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