02d76e6afae0e40826dc8eeff4272544841036c3 gperez2 Thu Aug 27 00:54:50 2026 -0700 Fixing "exomes and genomes variants" to "exome and genome variants" in the gnomAD v4.1.1 announcement image caption. refs #38166 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 12ca13960bd..604f23bb5cc 100644 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -87,31 +87,31 @@
  • gnomAD MPC (composite track): Shows a machine-learning score that predicts which missense variants are likely to be deleterious, computed from the gnomAD v4.1.1 release of 730,947 exomes. The score is shown as four allele-specific tracks (A, C, G, T).
  • gnomAD MPC overlaps: Covering the small subset of variants (about 250,000, or 0.4% of the ~70 million scored variants) that are scored against more than one transcript.
    • Genome Browser screenshot of the gnomAD v4.1.1 and MPC tracks -

    gnomAD v4.1.1 exomes and genomes variants, the LoF and missense +

    gnomAD v4.1.1 exome and genome variants, the LoF and missense constraint tracks, and the four gnomAD MPC allele tracks plus MPC overlaps, at the KCNH1 locus on hg38.

    For more information about the v4.1.1 update, see the gnomAD blog post.

    We would like to thank the Genome Aggregation Database Consortium for making these data available, and Kaitlin Samocha for providing the MPC score data. We would also like to thank Christopher Lee, Maximilian Haeussler, and Gerardo Perez for their efforts on this release.