How to contribute with WGS data representing population cohort from Slovakia?
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2
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29
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September 9, 2024
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Is joint (combined genome+exome) FAF unreliable if either genome or exome fails filters?
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2
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361
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September 6, 2024
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AB_MEDIAN field in older gnomad releases r2. and 3?
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1
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189
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September 6, 2024
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Rare and common variants numbers
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1
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166
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September 6, 2024
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Number of NFE male individuals in v2.1.1
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4
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205
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September 6, 2024
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Discrepant frequencies flag in VCF files?
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1
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142
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September 5, 2024
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chrX_mean_dp and chrY_mean_dp
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1
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186
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September 5, 2024
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Haplotype aggregated info
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1
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22
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September 5, 2024
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Multi-SNV Variant Type
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1
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261
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September 4, 2024
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gnomAD Copy number variants bed files
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3
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62
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September 3, 2024
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Difference between V2 and V4
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1
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61
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August 27, 2024
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Availability of ExAC WES BAM files
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1
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32
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August 22, 2024
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Query Regarding Overlap Between Exome and Genome Cohorts
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1
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32
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August 22, 2024
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Only need VCFs of healthy individuals
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1
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123
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July 29, 2024
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Number of variants in each vcf file
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2
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109
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July 23, 2024
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V4: Number of missense variants in VCFs doesn't match the stats
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1
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42
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July 23, 2024
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The Genetic Ancestry Group Frequencies table show Amish for v4.1 Exomes
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1
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34
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July 22, 2024
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PhyloP Question- Different on UCSC browser
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1
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105
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July 11, 2024
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GnomAD v3 random forest performance
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0
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79
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July 4, 2024
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Will there be a V4 non-cancer
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2
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111
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July 3, 2024
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List of variants databases
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1
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114
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July 2, 2024
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XX and XY sample numbers for v4 exomes and genomes
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1
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103
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June 28, 2024
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Congenital Heart Defects - Screened out?
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1
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66
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June 27, 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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81
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June 27, 2024
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Cannot complete (or even view) user survey
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2
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74
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June 20, 2024
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About allele balance
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2
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107
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June 5, 2024
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Ancestry inference params in v4
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1
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133
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June 5, 2024
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Variant allele frequency versus population frequency
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1
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331
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May 28, 2024
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High number of pathogenic variants in non-UKBB individuals
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1
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302
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May 24, 2024
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Missing MT variant VCF file for gnomAD-v4 or v4.1
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2
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155
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May 24, 2024
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