8c2f7318d8d821de9b2a25750586a94ab5e8c1bb lrnassar Fri Nov 15 18:50:19 2024 -0800 Giving the UI link cronjob some love by fixing all the 301 redirects. These are the bulk of the items listed on the cron. No RM. diff --git src/hg/makeDb/trackDb/human/encodePseudogene.html src/hg/makeDb/trackDb/human/encodePseudogene.html index 4b4c811..4fbf941 100644 --- src/hg/makeDb/trackDb/human/encodePseudogene.html +++ src/hg/makeDb/trackDb/human/encodePseudogene.html @@ -84,31 +84,31 @@ All pseudogenes in the list have been extensively curated by Adam Frankish and Jennifer Harrow at the The Wellcome Trust Sanger Institute.
More information about this data set is available from pseudogene.org/ENCODE.
This track shows pseudogenes annotated by the -HAVANA group +HAVANA group at the Wellcome Trust Sanger Institute. Pseudogenes have homology to protein sequences but generally have a disrupted CDS. For all annotated pseudogenes, an active homologous gene (the parent) can be identified elsewhere in the genome. Pseudogenes are classified as processed or unprocessed.
Prior to manual annotation, finished sequence is submitted to an automated analysis pipeline for similarity searches and ab initio gene predictions. The searches are run on a computer farm and stored in an Ensembl MySQL database using the Ensembl analysis pipeline system (Searle et al., 2004, Harrow et al., 2006).
A pseudogene is annotated