Differences for LC_pLoF flags between v4.1.0 and v2.1.1
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1
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95
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October 28, 2024
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gnomAD v4 - bottleneck populations?
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6
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468
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October 28, 2024
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Insertion and Deletion at the same position with flipped alleles
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1
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52
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October 28, 2024
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Inconsistent SNP MAF values between VCF v4.0 and browser
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5
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353
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October 28, 2024
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Variant QC SNV pass count v4
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7
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316
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October 28, 2024
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Is my interpretation of LOEUF threshold correct?
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1
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253
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October 15, 2024
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V4 vs v4-nonUKB CFTR F508del
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1
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99
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October 4, 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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102
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September 27, 2024
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Reasons for missing annotations
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1
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204
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May 1, 2024
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How to calculate MAPS score for gnomAD v4/v4.1?
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0
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43
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September 19, 2024
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dbSNP156 vs gnomAD WGS
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1
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106
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September 17, 2024
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Difference Between Gene Name and Genomic Position Queries in gnomAD
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1
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37
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September 17, 2024
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Spliceai_ds_max scores don't match spliceailookup
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2
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273
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September 16, 2024
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Geographical place of origin of samples
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1
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54
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September 11, 2024
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File containing binned methylation level of SNVs
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3
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53
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September 6, 2024
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How to contribute with WGS data representing population cohort from Slovakia?
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2
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33
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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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394
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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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195
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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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216
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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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223
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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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157
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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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193
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September 5, 2024
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Haplotype aggregated info
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1
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42
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September 5, 2024
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Multi-SNV Variant Type
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1
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282
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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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89
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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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92
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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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41
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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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39
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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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155
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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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154
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July 23, 2024
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