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/human/hg19/wgEncodeCaltechRnaSc.html src/hg/makeDb/trackDb/human/hg19/wgEncodeCaltechRnaSc.html index 3aacc7f7092..3fa7c243767 100644 --- src/hg/makeDb/trackDb/human/hg19/wgEncodeCaltechRnaSc.html +++ src/hg/makeDb/trackDb/human/hg19/wgEncodeCaltechRnaSc.html @@ -1,23 +1,23 @@

Description

This track is produced as part of the ENCODE Project. Describe the project here. A major goal of the ENCODE project is the complete characterization and understanding of the regulation and dynamics of the human transcriptome. High-throughput sequencing of reverse-transcribed RNA molecules (RNA-seq) has revolutionized work in this area by providing a genome-wide digital readout of transcription at base-pair resolution. However, such measurements are typically performed on population consisting of a large number of cells thus the readout is the average of the transcriptome profiles of individual cells. -This masks potentially important cell-to-cell variation in transcript abundance, allele expression bias, dynamic response to external stimuli, etc. In order to adress these issues, +This masks potentially important cell-to-cell variation in transcript abundance, allele expression bias, dynamic response to external stimuli, etc. In order to address these issues, we have generated single-cell RNA-seq measurements for invidual cells from ENCODE cell lines.

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Raw Signal
Density graph (wiggle) of read coverage.