LogoLogo
Illumina KnowledgeIllumina SupportSign In
  • Home
  • 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+)
    • Integrations
      • 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+)
  • 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 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
      • 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
      • More release notes
        • 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
Powered by GitBook
On this page
  • Release highlights for both workbench 34.0 and pipeline 34.0:
  • Updates
  • Analysis Tools | Increase efficiency with new multiselect variants, viewed/unviewed variants and new preset filters on PrimateAI-3D, REVEL and more
  • i. Multiselect variants and bulk tag, assign pathogenicity and mark viewed
  • ii. New feature marks viewed/unviewed variants for increased analysis efficiency
  • iii. New preset filter feature: Keep AI Shortlist tagged variants in a preset filter even if tag is changed by user
  • iv. New preset filter capability: Filter on PrimateAI-3D score
  • v. New preset filter capability: Filter on REVEL score
  • vi. New preset filter capability: Filter variants using values in the DRAGEN VCF filter field, for example QUAL=PASS
  • vii. New preset filter capability: Filter variants where severity/main effect is unknown
  • Limitations
  • Organization Settings | Customize, manage & control your organization with these new features
  • i. Create and manage Presets and Preset Groups
  • ii. New ‘Move to Trash’ status replaces support archive request
  • iii. New organization settings configure default page, analysis table columns
  • Limitations
  • New Annotations: PrimateAI-3D, gnomAD v4
  • i. Emedgene now includes the newly published Illumina PrimateAI-3D prediction score!
  • II. gnomAD v4 is here!
  • Limitations:
  • Lab Tab | New case quality section, Peddy contamination, improved single gene coverage workflow
  • i. New Case Quality section in the Lab Tab
  • ii. Lab Tab | New Peddy contamination column
  • iii. Lab Tab | Workflow improvement – view single gene coverage metrics when analyzing a large panel
  • General Workflow Improvements: Support BAF, ROH for customers starting from VCF, display Curated data in IGV, improved login and performance for ILMN clouds, new export/report capabilities
  • i. Support ingestion of additional visualization files for customers starting from VCF via the API and batch upload (but not via the UI). These visualizations were already supported for customers starting from FASTQ (32.0 and up).
  • ii. Visualize Curate data! Visualize both SNV and SV Curated data within the IGV viewer
  • iii. Illumina cloud login improvements that will increase transparency on the selected domain and workgroup. This improves on current state where users are always logged into their previous workgroup regardless of the URL used.
  • iv. Add New Case | Batch Upload now supports
  • v. New frequently requested Export/Reporting fields have been added. Please contact your regional support team or techsupport@illumina.com if you’d like to modify your export/report.
  • vi. Analysis Tools | New export to csv capabilities
  • Limitations
  • Fixed Issues
  • Known Issues
  • Version update needed for access to new features
  • References

Was this helpful?

Export as PDF
  1. Release Notes
  2. Workbench & Pipeline Updates

New in Emedgene V34.0 (January 28th 2024)

Release highlights for both workbench 34.0 and pipeline 34.0:

  • Analysis Tools have gotten an efficiency boost with multiselect variants, variants marked as viewed, and frequently requested new preset filters capabilities.

  • Powerful new Organization Settings reduce your reliance on Illumina support, including Preset creation, management and validation and new Move to Trash status.

  • New annotations are available - Illumina’s high performing PrimateAI-3D prediction score and an update to the newly published gnomAD v4.

  • Lab Tab gets new case quality metrics, Peddy1 sample contamination, and view single gene coverage metrics.

  • Workflow improvements – more visualizations for customers starting from VCF, visualize Curate data (SNV and SV), improved login flow and report/export enhancements.

Emedgene customers can select their preferred version out of any of the past 5 releases. Customers on 29.0 and below should select an upgrade path at this time.


Updates

Patches
Date

August 13, 2024

August 6, 2024

June 19, 2024

May 17, 2024

May 5, 2024

April 18, 2024

Feb 21, 2024


Analysis Tools | Increase efficiency with new multiselect variants, viewed/unviewed variants and new preset filters on PrimateAI-3D, REVEL and more

i. Multiselect variants and bulk tag, assign pathogenicity and mark viewed

Increase the efficiency of your analysis by performing bulk actions on variants in the analysis tools. When hovering over any variant a checkbox will appear at the beginning of the row.

Actions available are:

  • Tag or clear tag from all selected variants.

  • Assign or clear pathogenicity from all selected variants.

  • Mark selected variants as viewed/unviewed

These actions are only available for non-finalized cases.

More bulk actions will be included in future versions.

The multiselect feature requires an update to Workbench 34.0.

ii. New feature marks viewed/unviewed variants for increased analysis efficiency

Some variants may appear in multiple preset filters. In order to increase analysis efficiency, variants will appear in bold if they have not been viewed, and will appear in regular font weight if they have been viewed. This clear visual indication on whether a variant was viewed or not will help users avoid reviewed variants more than once.

Viewed/unviewed status is tracked by user. If multiple users are analyzing a case, their viewed/unviewed activity is tracked separately. This activity can be modified via the multiselect tool.

Variant color and weight indicate the following:

The viewed/unviewed feature requires an update to Workbench 34.0.

iii. New preset filter feature: Keep AI Shortlist tagged variants in a preset filter even if tag is changed by user

The majority of Emedgene users begin their workflow by reviewing the AI Shortlist tagged ‘Most Likely’ variants. Prior to 34.0, once a user has changed the tag, for example to ‘In Report’, the variant would no longer appear in the most likely preset filter.

In this version we have added the capability to filter on AI Shortlist tagged variants independently of user tags. These variants will remain in the preset filter even when user modifies their tag. This will facilitate reviews of a case by multiple analysts.

The keep AI Shortlist tagged variants in filter feature requires an update to Workbench 34.0.

iv. New preset filter capability: Filter on PrimateAI-3D score

Presets can now be set to filter on both PrimateAI-3D scores and PrimateAI-3D predictions. Define a preset to show only variants with a PrimateAI-3D score value greater than a selected threshold and/or define a preset to display variants with a PrimateAI-3D prediction of either D (Damaging) or B (Benign).

This new capability can only be implemented through support teams and is not available from the user interface.

The PrimateAI-3D filter feature requires an update to both Workbench 34.0 and Pipeline 34.0.

v. New preset filter capability: Filter on REVEL score

Presets can now be set to filter on variants with a REVEL score value greater than a selected threshold.

This new capability can only be implemented through support teams and is not available from the user interface.

The REVEL filter feature requires an update to both Workbench 34.0 and Pipeline 34.0.

vi. New preset filter capability: Filter variants using values in the DRAGEN VCF filter field, for example QUAL=PASS

Presets can now be set to filter on DRAGEN VCF filter fields. These presets are exact match, text based. Multiple values can be selected, with an OR applied between them.

This new capability can only be implemented through support teams and is not available from the user interface.

The DRAGEN QUAL filter feature requires an update to both Workbench 34.0 and Pipeline 34.0.

vii. New preset filter capability: Filter variants where severity/main effect is unknown

Presets can now be set to filter on severity/main effect when those fields return an unknown value. This will help create filters for intergenic regions and speed analysis of genomes.

This new capability can only be implemented through support teams and is not available from the user interface.

The DRAGEN QUAL filter feature requires an update to Workbench 34.0.

Limitations

  • Some new preset filter capabilities can only be configured by Illumina support teams and are not available from the UI yet. Future versions will make them configurable from the UI.

  • The new Multiselect feature is only available for cases that have not been finalized.

  • Multiselect is limited to 50 variants at a time.

  • Multiselect activity record is for every variant individually, no aggregated activity.

  • Mark viewed variants is limited to 5000 variants per user per case, and the API can send 50 at a time.


Organization Settings | Customize, manage & control your organization with these new features

This version introduces new features allowing customers to customize, manage and control their organization without requesting Illumina support. We focused on the most requested features and will progressively enhance the organization tab to cover all configurable organization settings.

i. Create and manage Presets and Preset Groups

Presets are combinations of Filters that serve to implement your interpretation Standard Operating Procedures (SOP) within the Emedgene software. Each Preset filter represents an analysis step, and there is full traceability on which presets have been reviewed by your various team members.

A Preset Group is a combination of Preset filters in a particular order that represents a case analysis workflow. Multiple Preset Groups can be created and used for the analysis of different case types. Preset Groups are designed to adhere to laboratory analysis standards while increasing analysis efficiency.

Up to 34.0, the Preset filters have been implemented to your requirements by Illumina support teams.

Starting in 34.0 you can save your own Presets, Preset Groups and also migrate existing Presets into the new self-managed feature.

As part of this new feature, an automatic and comprehensive schema validation covering over 120 fields and their associated unique values was added for Presets and Preset Groups to ensure validity across organizations.

As always, these new features require specific roles which you can distribute to select team members.

  • Save Presets:

Saving Preset filters is simple.

  1. Apply any filtration strategy using any of the available filters in either simple or advanced mode.

  2. Click on the three-dot icon and select "Save as preset." Enter a unique name for the Preset (Note: Avoid using non-Latin symbols that don't follow the ISO-5589-1 standard).

  3. Don’t forget to save!

  • Preset and Preset Group management

A new Lab Workflow tab is now available in the the Organization Settings (click on your initials in the upper right to reach all settings).

In this tab you will be able to:

  • Manage Presets

  • Manage Preset Groups

  • Set a default Preset Group for your organization

a. Manage Presets

This card enables you to perform the following actions on your Presets:

  • Add New – will redirect you to the analysis tools to create a preset filter as described above.

  • View Preset contents by pressing on the arrow to the left of the Preset name.

  • Lock Preset – locked Presets cannot be edited or deleted.

  • Delete Preset – Delete a Preset that is not locked and has not been used in a case analysis. Once a Preset has been used in an in-use Preset Group it cannot be deleted, in order to maintain access to the case.

b. Manage Preset Groups

This card contains the Preset Group and Legacy tabs.

Preset Group allows you to perform the following functions on your Preset Groups, which are defined combinations of Presets which will be reviewed in a particular order.

  • View all existing Preset Groups for your organization.

  • View the contents of each Preset Group in the table, revealing the list of presets it contains.

  • Create and edit new Preset Groups:

  • Select a name (Note: Avoid using non-Latin symbols that don't follow the ISO-5589-1 standard and ‘Default’ and ‘Presets’ are restricted names and cannot be used).

  • Add and remove Presets from the Preset Group. A search functionality has been added for ease of use.

  • Reorder a list of Presets within the Preset Group.

  • Hide/unhide Preset Groups in the table for clear visibility on latest versions available for use. Note that hidden Preset Groups will not affect cases run with them, and when editing a case with a hidden Preset Group it will still be available.

c. Set a default Preset Group

A default Preset Group for your organization can be set and will be used for all cases without a selected Preset Group.

d. Migrating V1 Legacy Presets to V2 Preset Groups

We highly recommend performing the migration with the assistance of regional support teams.

At the time of your choice, you can elect to migrate your Preset Groups to the new Preset tool. The V1(legacy) tab will display a list of Preset Groups that are only available in the V1 schema and will require a migration activity to the new functionality.

To migrate:

  1. Download the JSON file available for the Preset Group in the legacy tab.

  2. Create a new Preset Group from file and upload the JSON file.

The migration tool will create all Presets contained within the V1 Preset Group, and also order them correctly in the V2 Preset Group.

The V2 Preset Groups have been migrated to a robust schema and the preset import will automatically run a schema validation on over 120 simple and complex fields along with associated values. This robust and automatic schema validation will ensure your Presets and Preset Groups function as expected after the transition.

If any errors are found during the automated validation of any single Preset, the migration will fail and no new Preset Group will be created. A clear error message regarding the Preset that was incorrectly formatted will be provided, at which point you can correct the error and re-upload. We recommend utilizing Illumina regional support teams to correct any such errors.

e. Using both V2 and V1 Preset Groups

If at any point in time you have both V1 and V2 Preset Groups available, you can select either when adding a new case.

When a legacy Preset Group was migrated to the new schema, only the V2 Preset Group will be presented.

f. Migrating Preset Groups from Staging to Production organizations

At any time, you can download a Preset Group from a staging organization, and create a new Preset Group from file in the Production organization.

Note that any Presets utilizing gene list IDs or tags will need to be modified in the production organization.

  • An error message will appear on gene list IDs, providing the Preset Groups were migrated in the same region. If migrating from one cloud to another, please search and replace all gene list IDs.

  • Please recreate tags in your Production organization before importing the Preset Group.

The Save/Manage/Migrate Presets and Preset Groups feature requires an update to Workbench 34.0.

ii. New ‘Move to Trash’ status replaces support archive request

Customers can now move cases ready for deletion to the new ‘Move to Trash’ status. This functionality replaces the request to archive cases via Illumina support teams.

Cases in ‘Move to Trash’ status are locked for editing, and only users with the correct roles can move them to another status.

Future versions will enable customers to automate deletion of cases in the ‘Move to Trash’ status according to selectable parameters.

The Move to Trash feature requires an update to both Workbench 34.0.

iii. New organization settings configure default page, analysis table columns

The new organization settings require an update to both Workbench 34.0.

Limitations

  • Some existing Preset functionality is only available via Illumina support teams – exclude benign, filtering on specific prediction scores and more. Please continue to work with your support team to implement these. Note that the newly introduced schema validation applies to all Preset functionality and any functionality added by support teams will undergo an automated validation.

  • The additional functionality will be exposed to customers starting in mid-2024 versions.

  • Complex Preset Groups (or/not conditions between filters) will be added in later 2024 versions. The most commonly requested exclusion of benign variants in Presets is possible today with the assistance of Illumina support teams.


New Annotations: PrimateAI-3D, gnomAD v4

i. Emedgene now includes the newly published Illumina PrimateAI-3D prediction score!

PrimateAI-3D is a deep-learning network trained on 4.5 million common genetic variants from 233 primate species. This state-of-the-art classifier accurately quantifies missense variant pathogenicity in humans, which improves discovery of genes affecting clinical phenotypes.

PrimateAI-3D has been added to the In Silico prediction scores card on the Variant Page. It provides both a numerical score and also a prediction, which can receive the value D (damaging) or B (benign) per variant. The prediction is based on both the score and the gene, score range for damaging/benign is different per gene.

Emedgene users can also create presets based on either the score or the prediction, and also include either or both in their export.

The PrimateAI-3D feature requires an update to both Workbench 34.0 and Pipeline 34.0.

II. gnomAD v4 is here!

On Emedgene, this dataset replaces both the gnomAD Genome V3 and the gnomAD Exome v2 Liftover data.

gnomAD links have been updated in 32.0 and above.

The gnomAD v4 feature requires an update to both Workbench 34.0 and Pipeline 34.0.

Limitations:

  • Note that since the gnomAD MID population has less than 1000 samples so it is not taken into account as a valid source.


Lab Tab | New case quality section, Peddy contamination, improved single gene coverage workflow

i. New Case Quality section in the Lab Tab

For all cases with a number of genes above a customer defined threshold, Emedgene performs an additional case quality check. Up to 34.0, results of this quality check were not made available to customers and any failure would cause the case to fail and trigger an Illumina support investigation. Starting with this version, cases will not fail, and the result of the case quality check will be provided to users, so they can determine whether to continue with the analysis.

The Case Quality section contains:

  1. Gene list threshold: reflects the gene list threshold applied for the case quality check (default: 50).

  2. A table displaying the results of the various validations performed:

  • GnomAD Validation - Ensures that each chromosome contains a minimum of 1 variant annotated with GnomAD. Importantly, this validation applies only to chromosomes with at least 100 SNV variants within defined Kit or coding regions. Possible values are Succeed, Failed, Skipped.

  • ClinVar Validation - Ensures that each chromosome contains a minimum of 1 variant annotated with ClinVar. Importantly, this validation applies only to chromosomes with at least 100 SNV variants within defined Kit or coding regions. Possible values are Succeed, Failed, Skipped.

  • Auto Analysis Validation – Ensures that at least one variant was tagged by the Emedgene AI. This validation will not apply in cases with a gene list below the defined threshold. Possible values are Succeed, Failed, Skipped.

  • Chromosome Validation – Ensures that each chromosome contains a minimum of 1 variant with high quality. Importantly, this validation applies only to chromosomes with at least 100 SNV variants within defined Kit or coding regions. Possible values are Succeed, Failed, Skipped.

  • mtDNA Reference Validation – Ensures that the rCRS reference was used for mtDNA variants. If no mtDNA variants are present in the case the check will receive a Succeed value. Possible values are Succeed, Failed.

When one of the Case Quality checks fails, both the section and the Lab Tab will display an alert.

The Case Quality feature requires an update to both Workbench 34.0 and Pipeline 34.0.

ii. Lab Tab | New Peddy contamination column

A new column titled ‘Contamination’ will display the following values:

  • Yes - IDR_BAF >=0.300

  • Likely - 0.241<= IDR_BAF <0.300

  • Unlikely - 0.200<= IDR_BAF <0.24

  • No - IDR_BAF <0.200 but not 0

  • N/A - IDR_BAF = 0.000 or no data is available for this sample (old case)

IDR_BAF is the inter-decile range (90th percentile - 10th percentile) of the b-allele frequency. Peddy analyzes a distribution of all sites of alts / (ref + alts) and then reports the difference between the 90th and the 10th percentile. Large values indicated likely sample contamination.

When hovering over the value a tool tip will also display the HET ratio (proportion of sites that were heterozygous) and the HET count (number of heterozygote calls in sampled sites).

The Peddy contamination feature requires an update to both Workbench 34.0 and Pipeline 34.0.

iii. Lab Tab | Workflow improvement – view single gene coverage metrics when analyzing a large panel

Users can now remove all genes in a large gene panel, to quickly search and view for a single gene.

The single gene coverage enhancement requires an update to Workbench 34.0.


General Workflow Improvements: Support BAF, ROH for customers starting from VCF, display Curated data in IGV, improved login and performance for ILMN clouds, new export/report capabilities

i. Support ingestion of additional visualization files for customers starting from VCF via the API and batch upload (but not via the UI). These visualizations were already supported for customers starting from FASTQ (32.0 and up).

  • BigWig TNS (Tangent Normalized Signal) – The TNS track simplifies and increases reliability of CNV analysis and is available for customers running WGS. File supported: tn.bw.

  • B-Allele Frequency BigWig – The track aids in CNV and LOH analysis and is available for WES and WGS samples. File supported: baf.bw.

  • ROH BED file – The Regions of Homozygosity (ROH) plot is a visualization of homozygosity that may suggest the presence of uniparental isodisomy or partial isodisomy and is available for customers running WGS. File supported: roh.bed.

This feature requires an update to Workbench 34.0.

A summary of accepted DRAGEN 4.2 outputs in 34.0:

ii. Visualize Curate data! Visualize both SNV and SV Curated data within the IGV viewer

  • Curate SNV and Curate SV tracks are available in addition to the ClinVar tracks that were already available

  • Colors indicate variant pathogenicity:

    • Green = Benign/Likely Benign

    • Yellow = VUS

    • Red = Pathogenic/Likely Pathogenic

    • Black = Conflicting interpretation of pathogenicity

    • Grey = No assertion provided.

This feature requires an update to Workbench and Pipeline 34.0.

iii. Illumina cloud login improvements that will increase transparency on the selected domain and workgroup. This improves on current state where users are always logged into their previous workgroup regardless of the URL used.

  • Logging in to any Emedgene URL on Illumina cloud will first direct you to select your domain, in case a user is active in multiple domains, and then to select a possible workgroup. Workgroups will be displayed if the Emedgene application is assigned, they are part of the domain, and the user logging in belongs to the workgroup.

  • No need to remember a URL, you can login through app.emg.illumina.com and you will be directed to your domain and workgroup automatically.

  • If no URL has been assigned to a workgroup, domain admins and workgroup owners can initiate a URL assignment workflow.

  • Select the following parameters

    • The region your domain is in

    • A URL pattern from the list of available patterns

    • A platform version. If a URL is in use with a platform version, only that version will be available for the selected URL.

    • Both the URL pattern and the platform version can be changed from the Organization Settings later.

This feature requires an update to Workbench 34.0.

iv. Add New Case | Batch Upload now supports

  • Commas within any cell

  • Whitespace, semicolons & separated values will be ignored and information will be extracted regardless.

This feature requires an update to Workbench 34.0.

  • Case Level: List of genes with insufficient region based on coverage or BaseGT (for cases that have a gene list applied at case creation)

  • Case Level: Sequencing lab information, sample quality metrics and pedigree metrics.

  • Variant Level: SNV and CNV ACMG section.

This feature requires an update to Workbench 34.0.

vi. Analysis Tools | New export to csv capabilities

  • Exports each missense prediction result as a separate columns: Polyphen2 HDIV, Polyphen2 HVAR, SIFT, MutationTaster, LRT, DANN, REVEL, PrimateAI-3D score, PrimateAI-3D Prediction.

  • Export of Zygosity for Mother and Father as separate columns, in addition to Proband Zygosity and Other family members Zygosity.

  • Exports disease inheritance mode (from Disease column).

  • Exports "variant inheritance" – can have several values separated.

This feature requires an update to Workbench 34.0, but PrimateAI-3D and REVEL require a pipeline update.

Limitations

  • CNV variants larger than 20 Mbp are not annotated with genes name and effect, these variants are shortlisted by default by the AI Shortlist, but ACMG automation is not applied to them.

  • There is still a feature discrepancy for customers running DRAGEN through Emedgene (starting from FASTQ) or outside of Emedgene (starting from VCF).

  • Export to excel is limited to 32KB in size, which may prevent exports with very large CNVs.

  • API | No complex sorting via API is possible yet, only on a single column.


Fixed Issues

  • Add New Case | Network | Default consent is ‘restricted’.

  • Add New Case | Batch Upload | Fixed error where customers received a ‘Not Authenticated’ due to a timeout for large uploads.

  • Add New Case | Fixed an issue for API/batch/UI users trying to create a case from BSSH with 15-20 sample files would timeout.

  • Add New Case | Ordering portal users do not see Network Sharing fields, previously they could see but not edit them.

  • Lab Tab, Sidecar | Pedigree | Fixed issue where in very large pedigrees some family members can’t be clicked to view quality.

  • Candidates | Fixed a bug when clicking on See all candidates link, variant filters were inactivated.

  • Candidates | Fixed issue where SV Insertions information was partially displayed.

  • Variant Page | Visualization | Fixed an UI issue where IGV window was out of frame.

  • Variant Page | ACMG SNV Score | Fixed but where incorrect score was showing for mtDNA variants, although classifier behaves as expected.

  • Variant Page | Fixed issue where zygosity can’t be edited in the Sanger confirmation component.

  • Cases Page | Fixed issue where contact support link for failed cases did not work.

  • Report/Export | Fixed issue where variants tagged as ‘Most Likely’ order was not preserved when pushing to the report.

  • Report/Export | Fixed issue in miniVCF header blocking subsequent analysis in other tools.

  • Activity | Fixed issue where long names were not displayed properly.

  • Pipeline | Multiple improvements to avoid pipeline failures due to unavailable files and resources.

  • Infrastructure | Multiple improvements of resource allocations to increase robustness and performance.


Known Issues

  • Add New Case | Batch Upload | Analysis Type field is not available with this version of Batch Upload, and it cannot be used to initiate the new Carrier workflow.

  • Add New Case | Create a case from case creation summary does not work, please click on top Add New Case button from cases page.

  • Add New Case | For customers starting from Joint gVCF, please make sure the proband is first in order to see the correct insufficient region calculation.

  • Add New Case | Test type ‘Other Test’ is not supported on Illumina clouds yet.

  • Add New Case | API | When sending due date please use UTC time, customer time zone is not taken into account with API, only through the UI.

  • Reanalysis | If HPO terms were updated between analyses, the reanalysis will not automatically map previous HPO terms to new ones.

  • Lab Tab | Reanalyzed cases will show up with duplicated insufficient gene regions.

  • Lab Tab | STR repeats number for parents does not exist, proband values displayed.

  • Lab Tab | Insufficient coverage export will not work via UI or API if an included gene does not have a start or end position in NCBI.

  • Candidates | Gene name displayed on candidate page can be different than pipeline and variant Page.

  • Candidates Page | Compound het SNV-CNV variants will not display the automated CNV classification. Workaround – view variants from analysis table.

  • Evidence Graph | LitVar links will not work due to a change in the LitVar link structure.

  • Variant Page | Clinical Significance | When a disease has both an OMIM and a CGD source, the CGD inheritance modes mistakenly override OMIM inheritance modes.

  • Variant Page | Visualization | Chromosome ideogram visualization is missing for mtDNA variants in VCF case run on GRCh37.

  • Variant Page | Visualization | Simple/Advanced selectors will not work for locally uploaded BAM files.

  • Variant Page | Visualization | Zoom out of BigWig/TTS displays mean data.

  • Variant Page | Visualization is not supported for users storing VCF and CRAM on ICA V1 and BSSH. Only VCF and BAM are supported.

  • Variant Page | Manually Added Variants | Users without the role can add variants but not save them. Button should be disabled.

  • Variant Page | Transcript selection in fusion genes may be blocked since only a transcript for a single gene can be selected.

  • Analysis Tools | Preset Filters | Preset containing a gene list ID will display filtered data when an organization has configured a base gene list filter.

  • Analysis Tools | ‘Last’ button on pagination does not work.

  • Organization Settings | Set mandatory fields - does not work from the UI. Please contact support if you’d like to configure these fields for your account.

  • Organization Settings | Gene Lists | Very large gene lists (>6700 genes) may return a false error message during creation, despite being successfully created.

  • Network | GRCh37<-->GRCh38 Liftover not available for older components of Network infrastructure, as a result, [Variant Page | Clinical Significance | Networks Classified] may remain erroneously empty while [Variant page | Related cases section] shows relevant information. Same gap for manually classified variants.

  • Network | Zygosity, even when set in extended sharing, may remain blank for older cases. Once you click on a case missing zygosity it will be saved for all future views.

  • ILMN Clouds | Help Center | Some links may not work. Work around: Paste the title into the help center search.

  • Curate | ILMN cloud users need to be logged in to the organization from which they are trying to access Curate.

  • Curate | Discrepancy between Analyze and Curate HGVS parser may be experienced.

  • API | Assign users to case fails with no error if faulty emails used.

  • API | Creation of large gene lists may return an error (due to timeout) despite the creation of the gene list.

  • API | Marking over 5000 variants as viewed will not result in an error message, although this is the database limitation for saving viewed variants.

  • API | Swagger | Authorize function returns a 400 error.

  • Webhooks | Not functioning for software case status changes.

  • Activity | Editing interpretation paragraph yields an erroneous activity labeled reanalysis.

  • Dashboard | Diagnostic Yield includes Uncertain as Resolved.


Version update needed for access to new features

Feature

Workbench 34.0

Pipeline 34.0

Analysis Tools / Multiselect

✅

❌

Analysis Tools / Viewed/Unviewed

✅

❌

Analysis Tools / Presets / Keep AI Shortlist tagged variant in preset even if tag changes

✅

❌

Analysis Tools / Presets/ Filter on PrimateAI-3D

✅

✅

Analysis Tools / Presets / Filter on REVEL score

✅

✅

Analysis Tools / Presets / Filter on DRAGEN QUAL=PASS

✅

✅

Analysis Tools / Presets / Filter on variants with severity/main effect unknown

✅

❌

Organization Settings / Manage Presets & Preset Groups, inc migration from v1 to v2 schema

✅

❌

Organization Settings / Default page & analysis tools columns settings

✅

❌

Case / Move to Trash status

✅

❌

Annotations / PrimateAI-3D

✅

✅

Annotations / gnomAD v4

✅

✅

Lab Tab / Case quality & no fail sanity check

✅

✅

Lab Tab / Peddy contamination

✅

✅

Lab Tab / Remove all genes to view single gene coverage

✅

❌

ANC / Support BigWig TNF, BigWig BAF, ROH BED for customers starting from VCF

✅

❌

Variant Page / Visualization / Curate variant tracks for SNV, SV

✅

✅

Login / ILMN clouds / workgroup selection

✅

❌

Export / Genes in insufficient regions, sequencing lab, sample quality metrics, pedigree metrics, ACMG

✅

❌

Export / CSV / Missense predictions, zygosity additional columns, disease, inheritance

✅

Pipeline is required for PrimateAI-3D and REVEL exports. All else, Workbench only


References

PreviousV35 PatchesNextV34 Patches

Last updated 5 months ago

Was this helpful?

In order to revise your preset filters to this new capability, please contact your regional support team or reach out to .

Case Deletion is still a request via , please request that Illumina delete all cases in ‘Move to Trash’ status.

PrimateAI-3D demonstrated superior performance across 6 datasets in this publication:

Learn more about .

was published on November 1st, 2023 and we’re excited to make it available in this release so quickly. It contains data from 807,162 total individuals and is nearly 5x larger than the combined v2/v3 releases, and more diverse. Both the exome callset (730,947 individuals) and the genome callset (76,215 individuals) were aligned to build GRCh38 of the human reference genome.

While the case quality check can identify issues with exome and genome cases, it can often be falsely triggered for small panel cases, and it is recommended to exclude it for these cases by setting an appropriate gene threshold. Panels carved out with BED files can also be excluded, please contact your regional support teams or to set up this exclusion.

The Lab Tab will now display the results of the Peddy assessment of sample contamination (PMID: ), which calculates a deviation using all the sample alt-alleles, providing a sample specific contamination estimation that can detect human and bacterial contamination.

v. New frequently requested Export/Reporting fields have been added. Please contact your regional support team or if you’d like to modify your export/report.

Pedersen and Quinlan, Who’s Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy, The American Journal of Human Genetics (2017),

techsupport@illumina.com
techsupport@illumina.com
Science
PrimateAI and view publications
gnomAD v4
techsupport@illumina.com
28190455
techsupport@illumina.com
http://dx.doi.org/10.1016/j.ajhg.2017.01.017
V34.7
V34.6
V34.5
V34.4
V34.3
V34.2
V34.1