V37 Patches

Patches

Date

V37.3

May 25, 2025

V37.2

April 6, 2025

V37.1

March 5, 2025

Pipeline | DRAGEN 4.3 Targeted | Fixed a rarely occurring issue where SMN variants are duplicated.
Genome View | Changed the default scale for the LogR/TNS track from -2 to 2 (instead of -3 to 3) based on customer usability feedback.
Variant Page | Variant interpretation box | Fixed an issue causing long load time to make the interpretation available for editing.
Variant Page | Summary | Fixed an issue where ACMG classification changes were not updated to summary tab.
Variant Page | Evidence | Fixed an issue where ACMG reclassify button was active even when the variant is not eligible for reclassification.
Settings | Presets | Fixed an issue in preset v1 to v2 migration that converted some numbers to their scientific notation.
Settings | Presets | Fixed an issue in preset v1 to v2 migration that caused filters to reorder when having a duplicated name.
Curate | Unified variant validations to a single mechanism for consistency from Analyze and Curate. Curate now accepts variants with unknown positions (both for protein and coding), which are represented in HGVS by "?".
Propagations from 35.7, 35.8 and 36.6.

Add New Case | BSSH Integration | Will pass QcPassed, and also Undefined datasets if no QcPassed are available.
Pipeline | Fixed an issue causing cases to be delivered with no AI results after a failure/rerun.
AI Shortlist | Fixed an issue where AI did not prioritize variants in an organization’s curated genes if they are Genes of Unknown Significance.
Analysis Tools | Presets | Added support for Array calling methodology in Quality Filters.
Analysis Tools | Filters | Fixed a UI issue where for Polymorphism Advanced filters indicators were not aligned with selection.
Variant Page | Evidence | Fixed an issue where ACMG classification evidence text was misaligned with actual calculation.
Organization Settings | Fixed a UI issue where if a dot appears in file name, file type always shown as text.
Report/Export | HGNC IDs are also available for CNVs.
Propagations from 35.7 and 36.5.

Pipeline | For integrated DRAGEN analyses running on ICA via the ICA runner component, improved integration stability.
Genome View | Added a warning that in the genome view, only the largest 500 variants are displayed.
Analysis Tools | Fixed an issue where prediction score filters were intermittently not working for panel cases in v37.0.
Analysis Tools | Fixed an issue where search by position in preset filters for GRCh38 was not working in v37.0.
Analysis Tools | Fixed an issue where preset filters were showing an error message even if filters are retrieved.
Curate | Now supports the import of start loss variants (p.Met1?).
Propagations from 35.6 and 36.4.

Last updated 6 days ago

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Patches

Date

V37.3

May 25, 2025

V37.2

April 6, 2025

V37.1

March 5, 2025

Pipeline | DRAGEN 4.3 Targeted | Fixed a rarely occurring issue where SMN variants are duplicated.
Genome View | Changed the default scale for the LogR/TNS track from -2 to 2 (instead of -3 to 3) based on customer usability feedback.
Variant Page | Variant interpretation box | Fixed an issue causing long load time to make the interpretation available for editing.
Variant Page | Summary | Fixed an issue where ACMG classification changes were not updated to summary tab.
Variant Page | Evidence | Fixed an issue where ACMG reclassify button was active even when the variant is not eligible for reclassification.
Settings | Presets | Fixed an issue in preset v1 to v2 migration that converted some numbers to their scientific notation.
Settings | Presets | Fixed an issue in preset v1 to v2 migration that caused filters to reorder when having a duplicated name.
Curate | Unified variant validations to a single mechanism for consistency from Analyze and Curate. Curate now accepts variants with unknown positions (both for protein and coding), which are represented in HGVS by "?".
Propagations from 35.7, 35.8 and 36.6.

Add New Case | BSSH Integration | Will pass QcPassed, and also Undefined datasets if no QcPassed are available.
Pipeline | Fixed an issue causing cases to be delivered with no AI results after a failure/rerun.
AI Shortlist | Fixed an issue where AI did not prioritize variants in an organization’s curated genes if they are Genes of Unknown Significance.
Analysis Tools | Presets | Added support for Array calling methodology in Quality Filters.
Analysis Tools | Filters | Fixed a UI issue where for Polymorphism Advanced filters indicators were not aligned with selection.
Variant Page | Evidence | Fixed an issue where ACMG classification evidence text was misaligned with actual calculation.
Organization Settings | Fixed a UI issue where if a dot appears in file name, file type always shown as text.
Report/Export | HGNC IDs are also available for CNVs.
Propagations from 35.7 and 36.5.

Pipeline | For integrated DRAGEN analyses running on ICA via the ICA runner component, improved integration stability.
Genome View | Added a warning that in the genome view, only the largest 500 variants are displayed.
Analysis Tools | Fixed an issue where prediction score filters were intermittently not working for panel cases in v37.0.
Analysis Tools | Fixed an issue where search by position in preset filters for GRCh38 was not working in v37.0.
Analysis Tools | Fixed an issue where preset filters were showing an error message even if filters are retrieved.
Curate | Now supports the import of start loss variants (p.Met1?).
Propagations from 35.6 and 36.4.

Last updated 6 days ago

Was this helpful?