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About the Feature Requests category
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0
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1159
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August 27, 2016
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SNV De novo calling tool for cohort research at scale
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0
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21
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June 2, 2026
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Symbolic Alleles and Overlapping Variants
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2
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66
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December 12, 2025
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Using GPUs from HAIL
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1
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66
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November 17, 2025
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Export MT as PLINK2 pgen/pvar/psam
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5
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164
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September 3, 2025
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Plink_export of DS value
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1
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77
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July 15, 2025
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Adding samples incrementally
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4
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2335
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February 27, 2025
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Transparency (Alpha) in hl.plot.scatter
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0
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190
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December 8, 2023
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Future support of Elasticsearch version 8
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1
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239
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September 5, 2023
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Support importing phased BGEN files
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0
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285
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August 22, 2023
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Se in logistic 'firth' model
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4
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331
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July 11, 2023
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Can you support Illumina DRAGEN msVCF?
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3
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762
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July 5, 2023
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Interaction Test between SNP * Covariate for a Binary Outcome
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7
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813
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May 18, 2023
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How to capture summarize() outputs?
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3
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501
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April 27, 2023
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Ukbb_common documentation seems stale
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12
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490
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January 21, 2023
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Fail to read a T2T VCF
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8
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437
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January 7, 2023
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DNARecords integration?
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1
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408
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September 20, 2022
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Add option to make scans inclusive
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2
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383
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August 24, 2022
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Wilcoxon ranksum test
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7
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1166
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August 19, 2022
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Variant Quality Score Recalibration
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3
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2137
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July 27, 2022
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Mixed Model support
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2
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506
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July 26, 2022
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Runs of homozygosity
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2
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394
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July 22, 2022
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Window_by_locus not available
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2
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500
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June 20, 2022
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Annotating with CADD, gnomad, Clinvar & dbNSFP on UKB RAP
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7
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987
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May 25, 2022
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Extract sequence from reference genome
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2
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493
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May 17, 2022
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How to suppress hail info output
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2
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510
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April 11, 2022
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SNP Eff Annotation
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2
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561
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March 23, 2022
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[PRS analysis] Request for allele frequency harmonization and SNP matching features
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2
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794
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December 20, 2021
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ABHet ratio for variant level QC
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4
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1017
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September 22, 2021
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Implement Regenie
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3
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735
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August 26, 2021
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