f7cf3eee5dc2134d550c6b35b2fb250f65673341 max Tue Feb 3 01:55:53 2026 -0800 changes after code review, refs #37059 diff --git src/hg/makeDb/trackDb/human/varFreqs.html src/hg/makeDb/trackDb/human/varFreqs.html index 625e2c0bf0e..6d672bc37cb 100644 --- src/hg/makeDb/trackDb/human/varFreqs.html +++ src/hg/makeDb/trackDb/human/varFreqs.html @@ -58,38 +58,38 @@ and 12,519 with whole-genome sequencing (WGS). The data contains 32,559 trios and 8,895 quads (one sibling without autism), and 824 twins. The same frequencies shown here are also available publicly on the SFARI Genome Browser. See (SPARK et al, Neuron 2018) for details or the methods below on this page.
  • GenomeAsia Pilot (GAsP): Whole-genome sequencing data of 1,739 individuals from 219 population groups across Asia. See (GenomeAsia Consortium, Nature 2019) for details.
  • - Australia MRGB: + Australia MGRB: The Australian Medical Genome Reference Bank collected whole-genome sequencing data of 4,011 healthy elderly individuals who lived >=70 years, to make sure that the dataset is depleted of damaging genetic variants. Age and sex summary graphs are available from the MGRB website. - See (Lacaze Eur J Humn Genet 2019) for details. + See (Lacaze Eur J Hum Genet 2019) for details.
  • ALFA: The NCBI ALlele Frequency Aggregator pipeline computes allele frequencies from approved, unrestricted dbGaP studies and makes them publicly available through dbSNP. Its goal is to release frequency data from over one million dbGaP subjects to aid discoveries involving common and rare variants with biological or disease relevance. The R4 release includes 408,709 subjects and allele frequencies for 15.5 million rs sites, including nearly one million ClinVar variants. We converted the NCBI track hub to VCF format, the data is freely available. Genotype and associated individual-level data are accessible through the dbGaP authorized access request system.