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Pull requests: broadinstitute/gatk-sv
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Add Genomic Disorder CNV calling and VCF integration
#945
opened Jun 24, 2026 by
mwalker174
Collaborator
•
Draft
Documentation updates related to ScoreGenotypes
#928
opened Mar 10, 2026 by
epiercehoffman
Collaborator
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Eliminate stochasticity in Median Coverage calculation
enhancement
New feature or request
#867
opened Sep 9, 2025 by
kjaisingh
Collaborator
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Update RegenotypeCNVs.wdl GetRegenotype task
#839
opened Jul 10, 2025 by
knathamuni
Contributor
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Ignore sites with null GTs during de novo rate calculation
#810
opened May 9, 2025 by
epiercehoffman
Collaborator
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Update VM spot pricing in monitoring analysis scripts
#765
opened Jan 6, 2025 by
mwalker174
Collaborator
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Remove outliers across per-contig VCFs
#654
opened Mar 11, 2024 by
epiercehoffman
Collaborator
•
Draft
Workflow to apply NCR and reference artifact filters and remove zero-carrier sites
#653
opened Mar 8, 2024 by
epiercehoffman
Collaborator
•
Draft
Removed pairwise batch effect checks from WDL workflow
#617
opened Nov 9, 2023 by
shadizaheri
Contributor
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Extend functionality for outlier sample exclusion workflow
#496
opened Feb 11, 2023 by
RCollins13
Contributor
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