198c9b8daecc44fbda6a6494c566c723920f030a lrnassar Wed Mar 11 18:25:21 2026 -0700 Fixing a few hundred clear typos with the help of Claude. Some are less important in code comments, but majority of them are in user-facing places. I manually approved 60%+ of the changes and didn't see any that were an incorrect suggestion, at worst it was potentially uncessesary, like a code comment having cant instead of can't. No RM. diff --git src/hg/makeDb/trackDb/mouse/mm9/wgEncodeSydhTfbs.release3.html src/hg/makeDb/trackDb/mouse/mm9/wgEncodeSydhTfbs.release3.html index de75aed2245..3a82e2b5c95 100644 --- src/hg/makeDb/trackDb/mouse/mm9/wgEncodeSydhTfbs.release3.html +++ src/hg/makeDb/trackDb/mouse/mm9/wgEncodeSydhTfbs.release3.html @@ -14,31 +14,31 @@ these experiments are available for download.

Display Conventions and Configuration

This track is a multi-view composite track that contains multiple data types (views). For each view, there are multiple subtracks that display individually on the browser. Instructions for configuring multi-view tracks are here. This track contains the following views:

Peaks
Regions of signal enrichment based on processed data (normalized data from pooled replicates). Intensity is represented in grayscale, the darker shading shows higher intensity (a solid vertical line -in the peak region represents the the point with the highest signal). +in the peak region represents the point with the highest signal). ENCODE Peaks tables contain fields for statistical significance, including FDR (qValue).
Signal
Density graph (wiggle) of signal enrichment based on processed data.

Metadata for a particular subtrack can be found by clicking the down arrow in the list of subtracks.

Methods

Cells were grown according to the approved ENCODE cell culture protocols. For details on the chromatin immunoprecipitation protocol used, see Euskirchen et. al., (2007), Rozowsky et. al. (2009) and Auerbach et. al. (2009).