From d0911a04958a04042da02a334ccc528dae79cc17 Mon Sep 17 00:00:00 2001 From: zsloan Date: Fri, 27 Mar 2015 20:28:51 +0000 Subject: Removed everything from 'web' directory except genofiles and renamed the directory to 'genotype_files' --- web/tutorial/ppt/WebQTLDemo_files/slide0026_notes_pane.htm | 5 ----- 1 file changed, 5 deletions(-) delete mode 100755 web/tutorial/ppt/WebQTLDemo_files/slide0026_notes_pane.htm (limited to 'web/tutorial/ppt/WebQTLDemo_files/slide0026_notes_pane.htm') diff --git a/web/tutorial/ppt/WebQTLDemo_files/slide0026_notes_pane.htm b/web/tutorial/ppt/WebQTLDemo_files/slide0026_notes_pane.htm deleted file mode 100755 index 138a5dca..00000000 --- a/web/tutorial/ppt/WebQTLDemo_files/slide0026_notes_pane.htm +++ /dev/null @@ -1,5 +0,0 @@ -
Part 3.  Many investigators would like to discover the set of downstream targets of a gene of interest.

In a genetic and functional sense, that question can only be addressed effectively if there is genetic variation in the particular gene.  We know that Fos is an important transcription factor, but unless it is polymorphic between C57BL/6J and DBA/2J, then it cannot generate a genetic variance signal with which we can work. We can still study covariance of Fos and hundreds of other transcripts (an interesting exercise), but there are no genetic causes-and-effects.
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