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Is my interpretation of LOEUF threshold correct?
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1
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288
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October 15, 2024
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Number of variants in each vcf file
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2
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161
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July 23, 2024
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Constraint metric
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4
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125
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September 11, 2024
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Topic Loading chunk 595 failed.(missing: https://gnomad.broadinstitute.org/js/595-fc9ff4040fdf0d877f0b.js)
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1
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152
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August 14, 2024
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Will there be a V4 non-cancer
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2
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132
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July 3, 2024
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Number of expected and observed pLoF variants for CYP8B1 looks unusual
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4
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104
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September 27, 2024
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PhyloP Question- Different on UCSC browser
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1
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159
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July 11, 2024
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gnomAD Copy number variants bed files
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3
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92
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September 3, 2024
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Number of observed variants vs hail query (v4.1.0)
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3
|
98
|
September 7, 2024
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Variant Co-Occurrence table headings
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4
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81
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February 3, 2025
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dbSNP156 vs gnomAD WGS
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1
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111
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September 17, 2024
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Discrepancy between gnomAD and UK Biobank
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2
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88
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November 5, 2024
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Ancestry RF classifer code and scripts
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7
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64
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May 12, 2025
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gnomAD v4.1 not working?
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2
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80
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July 19, 2024
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Does gnomAD have access to the clinical status of individuals included in their data?
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1
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105
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September 5, 2024
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Can I find HGVS Consequence of variant ID in gnomad.vcf.bgz?
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3
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77
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January 10, 2025
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V4 vs v4-nonUKB CFTR F508del
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1
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109
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October 4, 2024
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Difference between V2 and V4
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1
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96
|
August 27, 2024
|
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gnomAD v.4.1 API?
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1
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87
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January 24, 2025
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Differences for LC_pLoF flags between v4.1.0 and v2.1.1
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1
|
100
|
October 28, 2024
|
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PhyloP indel scores
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1
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86
|
February 13, 2025
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pLoF Metrics by Gene TSV columns
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3
|
65
|
December 11, 2024
|
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Cannot complete (or even view) user survey
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2
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83
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June 20, 2024
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V4.1 Structural Variants BED files
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1
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80
|
July 29, 2024
|
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What is the estimated relative distribution of gnomAD ancestry groups in the global population?
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1
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91
|
June 27, 2024
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Rounding the frequencies in the browser
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3
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55
|
September 10, 2024
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File containing binned methylation level of SNVs
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3
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53
|
September 6, 2024
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Assistance with Querying Non-Synonymous Variants for Specific Transcript ID
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2
|
49
|
August 9, 2024
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Congenital Heart Defects - Screened out?
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1
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70
|
June 27, 2024
|
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Geographical place of origin of samples
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1
|
56
|
September 11, 2024
|
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Short range haplotype frequencies
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0
|
94
|
June 21, 2024
|
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Genome build used for gnomad v4.1
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1
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53
|
April 8, 2025
|
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Insertion and Deletion at the same position with flipped alleles
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1
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54
|
October 28, 2024
|
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Access to Download
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1
|
50
|
October 16, 2024
|
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Haplotype aggregated info
|
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1
|
45
|
September 5, 2024
|
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GnomAD v3 random forest performance
|
|
0
|
91
|
July 4, 2024
|
|
GnomAD SVs v4, X-chromosome: homozygous males
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1
|
65
|
November 5, 2024
|
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V4: Number of missense variants in VCFs doesn't match the stats
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|
1
|
53
|
July 23, 2024
|
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The Genetic Ancestry Group Frequencies table show Amish for v4.1 Exomes
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|
1
|
43
|
July 22, 2024
|
|
Validating exome CNV
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3
|
40
|
April 9, 2025
|
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Discordant variant observations between v2.1.1 and v4.1
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2
|
37
|
April 7, 2025
|
|
All-sites allele numbers by ancestry group?
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1
|
43
|
October 10, 2024
|
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How to extract and analyze variant sequences from gnomAD v4 exome VCF
|
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0
|
59
|
January 12, 2025
|
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Variant co-occurrence request for V4
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1
|
43
|
April 29, 2025
|
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How to find germine mutations associated with cancer v 3.1.2
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1
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38
|
January 8, 2025
|
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C4B variant, please help!
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1
|
45
|
February 20, 2025
|
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Availability of ExAC WES BAM files
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1
|
43
|
August 22, 2024
|
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How to contribute with WGS data representing population cohort from Slovakia?
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2
|
34
|
September 9, 2024
|
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Co-located variants
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|
1
|
38
|
December 3, 2024
|
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GnomAD EXOME FILTERED PPM1D Variant
|
|
1
|
40
|
November 12, 2024
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