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+)
    • 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
  1. Release Notes
  2. Workbench & Pipeline Updates
  3. New in Emedgene V35.0 (May 22nd 2024)

V35 Patches

Patches
Date

V35.7

April 9, 2025

V35.6

March 4, 2025

V35.5

February 4, 2025

V35.4

December 3, 2024

V35.3

September 4, 2024

V35.2

July 24, 2024

V35.1

June 25, 2024

V35.7 Update (April 9th, 2025)

  • Export/Report | Adding the ‘source_gene_map’ field to the JSON report/export.

V35.6 Update (March 4th, 2025)

  • Variant Page | Fixed an issue for some CNVs that resulted in an inactive Export to Curate button.

V35.5 Update (February 4th, 2025)

  • Pipeline | Fixed Curate annotation issue for CNV to support multiple variant annotations.

  • Pipeline | Fixed issue where ploidy estimation failures caused case failure instead of triggering a lab tab alert.

  • Pipeline | Fixed issue where lab tab quality check was incorrect when a case was reanalyzed with a new gene list.

  • Analysis Tools | Improving re-analysis notification for ROI changes.

V35.4 Update (December 3rd, 2024)

  • Login | Fixed an issue affecting SSO integrations in legacy Emedgene clouds.

  • Add new case | Fixed an issue uploading BSSH files from the UI.

  • Add new case | Reanalysis | Fixed an issue reporting on tagged variants that are not present in a case reanalysis due to changed input files.

  • Pipeline | Fixed issue resulting in failed ingestion of DRAGEN targeted.json where genotype is null.

  • Pipeline | Added support for ingestion of software only DRAGEN outputs.

  • Pipeline | Improving support of joint called files for Hom reference genotype in parents.

  • Pipeline | Fixed issue causing GATK cases to fail when they contain infinity value.

  • Analysis Tools | Preset Filters | Added support for the candidate gene query even when gene list is boosted.

V35.3 Update (September 4th, 2024)

  • Add New Case | Fixed an issue that caused Pending Sequencing workflows to fail in V35.

  • Edit Case | Fixed a bug that prevented saving and running edited cases that were opened on versions <V35.

  • Pipeline | Fixed an issue causing more frequent case failures in V35 due to incorrect infrastructure assignment to cases where BED selection for region of interest is larger than expected.

  • Analysis Tools and Report/Export | V35.0 added support for large CNVs (over 20M bp). This caused ‘case incompatible’ errors for some CNV filters and in exporting/reporting. This hotfix fixes both issues.

  • Curate | Batch upload – Fixed a bug that resulted in variants added to Curate via the batch uploader to only be available in the original reference, instead of in both with liftover-on-the-fly.

  • User Access | Fixed a bug causing users belonging to several domains to lose their roles when switching between domains.

  • Propagations of fixes from v34.6 and v34.7 including the ability to update an organization to gnomAD 4.1 non-UKB data for SNVs/indels.

V35.2 Update (July 24th, 2024)

  • Edit Case | Fixed a bug preventing a rerun of cases when original files are no longer available on BSSH.

  • Pipeline | Expanded RNA disease associated gene list in transcript selection logic. The genes added to the exception list are:

    • RNU7-1 RNA, small nuclear Aicardi-Goutieres syndrome 9

    • RNU4-2 RNA, U4 small nuclear 2

  • Pipeline: Multiple fixes to improve pipeline robustness and reduce failure rates.

  • Lab Tab | Fixed a bug resulting in no data loaded to the lab tab for new organizations.

  • Analysis Tools | Filters | Fixed a bug for Variant Effect Filters, when moving from simple to advanced, not all variant effects were available for filtering, which also caused a variant count discrepancy.

  • Analysis Tools | Preset Filters | Fixed a bug that always showed the description of removing polymorphic variants as ‘Display polymorphism: True’ although the behavior of the filter correctly removed the variants.

  • Variant Page | Embedded IGV | Improved IGV performance by reducing API calls when moving between variants.

  • Variant Page | Embedded IGV | Option to toggle embedded IGV off to improve performance for customers using external visualization tools.

  • Export | Fixed a bug failing the export of parental data for some customers.

V35.1 Update (June 25th, 2024)

  • Edit Case | Fixed an issue that could prevent reanalysis of cases that were created via API and were missing fields required in v35.

  • Cases Page | Fixed a rarely occurring issue where cases can be displayed with the good quality green icon even though they contain an insufficient coverage warning.

  • Analysis Tools | Filters | Fix an issue that caused frameshift indels to disappear from variant table when moving between simple and advanced mode in the quality filters.

  • Curate | Batch upload enhancement that will ensure all characters uploaded to Curate are supported in Analyze.

  • Curate | Curate now supports MNVs that are supported in Analyze, which are MNV indels only.

  • Curate | Fixed an issue that prevented genes with no gene metrics to be uploaded to Curate.

  • Propagations from V34.5.


PreviousNew in Emedgene V35.0 (May 22nd 2024)NextNew in Emedgene V34.0 (January 28th 2024)

Last updated 1 month ago

Was this helpful?