603a734862321da4d9bde067c47a4a13175acc02
mspeir
Thu Jul 23 09:24:22 2026 -0700
Changes to slide decks based on CR; Adding reveal.js to source tree, rather than using CDN, refs #37874 #37904
diff --git docs/browserSlideDecks.md docs/browserSlideDecks.md
index 6bdb6708de8..b06031c4b94 100644
--- docs/browserSlideDecks.md
+++ docs/browserSlideDecks.md
@@ -1,48 +1,49 @@
---
title: "UCSC Genome Browser Slide Decks"
---
This page collects training slides for the UCSC Genome Browser. Each slide deck
has been curated with a specific purpose, from basic navigation to interpreting
clinical variants. They are self-contained web decks: open one in any browser,
present it full-screen (press F), read the presenter notes
-(press S), or jump to any slide from its **Contents** page. Feel free
-to use them in your courses or local trainings.
+(press S, which opens them in a separate browser tab; close that tab
+when you are done with them), or jump to any slide from its **Contents** page.
+Feel free to use them in your courses or local trainings.
[Contact us](/contacts.html) to suggest new slide decks or improvements to the
current ones.
## Deck 1: UCSC Genome Browser Basics
Basic features and navigation of the
[main genome browser display](/cgi-bin/hgTracks): configuring tracks and display
-modes, reading the gene model, the track groups, viewing and extracting DNA, the
-Table Browser, aligning sequences with BLAT, and loading your own data as custom
-tracks, track hubs, and sessions.
+modes, reading the gene model, browsing the track groups, viewing and extracting
+DNA, querying the Table Browser, aligning sequences with BLAT, and loading your
+own data as custom tracks, track hubs, and sessions.
**[▶ Open the deck](/docs/slideDecks/tutorial1-basics/presentation/)**
· [Contents](/docs/slideDecks/tutorial1-basics/tableOfContents/)
## Deck 2: Cancer Data in the Genome Browser
An overview of the cancer and clinical databases hosted by the Genome Browser,
-organized by **somatic** and **germline** diagnosis and worked on the
-BRAF V600E example: CIViC, COSMIC, ClinVar, and TCGA Pan-Cancer for
-somatic variants, and GenCC, OMIM, and gnomAD for germline questions.
+organized by **somatic** and **germline** diagnosis CIViC, COSMIC, ClinVar, and TCGA
+Pan-Cancer for somatic variants, and GenCC, OMIM, and gnomAD for germline
+questions. These databases are explored with a consistent BRAF V600E example throughout.
**[▶ Open the deck](/docs/slideDecks/tutorial2-cancer/presentation/)**
· [Contents](/docs/slideDecks/tutorial2-cancer/tableOfContents/)
## Deck 3: Clinical Examples & Variant Interpretation
How to interpret a variant end to end: the **Recommended Track Sets**, the
regulatory and epigenetic context that non-coding variants need, worked germline
(BRCA2) and somatic (BRAF V600E) examples, expression, and AI
predictors such as AlphaMissense and SpliceAI.
**[▶ Open the deck](/docs/slideDecks/tutorial3-clinical/presentation/)**
@@ -58,22 +59,22 @@
non-coding and regulatory variants, structural variants (CNVs), and repeat
expansions.
**[▶ Open the deck](/docs/slideDecks/tutorial4-clinical-cases/presentation/)**
· [Contents](/docs/slideDecks/tutorial4-clinical-cases/tableOfContents/)
## Deck 5: Teaching with the Browser
Ready-made, interactive teaching modules from our
[Education portal](/training/education/): the central dogma (reading frames,
codons, splicing), variant effects (synonymous, missense, nonsense, frameshift),
and real disease and evolution case studies. Each module is a clickable session
-plus a short page, ready to drop into a lecture or assignment.
+plus a short description of that session and what it shows, ready to drop into a lecture or assignment.
**[▶ Open the deck](/docs/slideDecks/tutorial5-teaching/presentation/)**
· [Contents](/docs/slideDecks/tutorial5-teaching/tableOfContents/)