diff options
| author | zsloan | 2015-03-27 20:28:51 +0000 |
|---|---|---|
| committer | zsloan | 2015-03-27 20:28:51 +0000 |
| commit | d0911a04958a04042da02a334ccc528dae79cc17 (patch) | |
| tree | 3c48e2e937c1dbeaf00a5697c87ed251afa5c8f1 /web/dbdoc/IoP_SPL_RMA_0509.html | |
| parent | a840ad18e1fe3db98a359a159e9b9b72367a2839 (diff) | |
| download | genenetwork2-d0911a04958a04042da02a334ccc528dae79cc17.tar.gz | |
Removed everything from 'web' directory except genofiles and renamed the directory to 'genotype_files'
Diffstat (limited to 'web/dbdoc/IoP_SPL_RMA_0509.html')
| -rwxr-xr-x | web/dbdoc/IoP_SPL_RMA_0509.html | 99 |
1 files changed, 0 insertions, 99 deletions
diff --git a/web/dbdoc/IoP_SPL_RMA_0509.html b/web/dbdoc/IoP_SPL_RMA_0509.html deleted file mode 100755 index c9696221..00000000 --- a/web/dbdoc/IoP_SPL_RMA_0509.html +++ /dev/null @@ -1,99 +0,0 @@ -<!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0 Transitional//EN"> -<HTML><HEAD><TITLE>IoP Affy MOE 430v2 Spleen (May09) RMA</TITLE> -<META http-equiv=Content-Type content="text/html; charset=iso-8859-1"> - -<LINK REL="stylesheet" TYPE="text/css" HREF='/css/general.css'> -<LINK REL="stylesheet" TYPE="text/css" HREF='/css/menu.css'> -<link rel="stylesheet" media="all" type="text/css" href="/css/tabbed_pages.css" /> -<SCRIPT SRC="/javascript/webqtl.js"></SCRIPT> - -<SCRIPT SRC="/javascript/dhtml.js"></SCRIPT> - -<script src="/javascript/tabbed_pages.js" type="text/javascript"></script> - -</HEAD> -<BODY bottommargin="2" leftmargin="2" rightmargin="2" topmargin="2" text=#000000 bgColor=#ffffff > - -<TABLE cellSpacing=5 cellPadding=4 width="100%" border=0> - <TBODY> - <TR> - <script language="JavaScript" src="/javascript/header.js"></script> - </TR> - <TR> - <TD bgColor=#eeeeee class="solidBorder"> - <Table width= "100%" cellSpacing=0 cellPadding=5> - <TR> - - <!-- split from Here --> - <!-- Body Start from Here --> - <P class="title">IoP Affy MOE 430v2 Spleen (May09) RMA <br>Accession number: <A HREF="/webqtl/main.py?FormID=sharinginfo&GN_AccessionId=227">GN227</A> <A HREF="/webqtl/main.py?FormID=editHtml"> - <img src="/images/modify.gif" alt="modify this page" border= 0 valign="middle"></A></P> - -<blockquote> -<p class="subtitle">Summary:</p> -<p>Spleen mRNA expression levels are measured for 77 individual BXD RI mice from 24 different strains. The expressed gene set were characterised using the Affymetrix Mouse430_2.0 GeneChip which encompass over 34,000 known genes.</p> -<p class="subtitle">Animals and Tissue Used to Generate This Set of Data:</p> -<p>Female BXD mice were harvested between 8 and 12 weeks of age. The oestrus cycle of each mouse was determined by observing the status of the cells obtained from a vaginal swab by light microscopy. Mice were culled by cervical dislocation; the brain and spleen were harvested immediately and snap frozen on dry ice. Tissues were subsequently stored at -80°C. Individual mice were identified by strain, age and cage number and were assigned a unique sample identifier number at this stage.</p> -<p class="subtitle">RNA Extraction:</p> -<p>The spleens (average weight 0.1g) were homogenised individually in 1ml of TRIzol reagent per 100mg of tissue using a polytron homogenizer and a glass pestle and mortar. The polytron homogenizer was found to most quickly and efficiently disrupt the tough splenic tissue, giving rise to moderate yields of RNA of good quality with little contamination. - -Homogenates were chloroform extracted using 0.2ml of chloroform per 1ml of TRIzol. These were shaken vigorously by hand and separated with the aid of phase lock heavy tubes. 0.5ml of isopropanol per 1ml of TRIzol was added to retained aqueous phase at room temperature. This was then centrifuged at 4,000 x g for 30 minutes at 2-8°C. The pellet was washed with at least 1ml of 75% ethanol per 1ml of TRIzol used, and mixed by vortexing until the pellet came loose from the tube wall. This was then centrifuged at 4,000 x g for 10 minutes at 2-8°C. The pellet was air dried, dissolved in 100μl of RNase-free water and incubated at 55-60°C for 10 minutes. The RNA sample purity and concentration was determined by gel electrophoresis and spectrophotometry -</p> -<p class="subtitle">About the array platform:</p> -<p>The Affymetrix microarrays used in this investigation were the GeneChip ® Mouse Genome 430 2.0 Array which enables genome-wide expression analysis on a single array. These probe arrays contain over 45,000 probe sets which analyse the expression of over 39,000 transcripts and variants from over 34,000 well characterized mouse genes. Multiple probe pairs per probe set provide several independent measurements for every transcript, increasing accuracy and reproducibility. The probe sets were selected from sequences derived from GenBank®, dbEST, and RefSeq. The sequence clusters were created from the UniGene database and then refined by analysis and comparison with the publicly available draft assembly of the mouse genome from the Whitehead Institute Centre for genome Research.</p> - -<p class="subtitle">eQTL Statistics:</p> This data set generates eQTLs with peak LRS scores of about 80 (see 1458092_at, Gene Symbol: Ap3m1). This is an impressive value given the sample size consists of only 23 BXD strains. A total of 194 probe sets are associated with LOD > 10 or LRS >46. - - -<p class="subtitle">Researchers:</p> -<p>Sarah Lawn under the supervision of Cathy Fernandes, Leo Schalkwyk and Steve Whatley.</p> -<p class="subtitle">Publications:</p> -<p>Davies, M.N., Lawn, S., Whatley, S., Fernandes, C., Williams, R.W., Schalkwyk, L.C. (2009). , Is blood a reasonable surrogate for brain in gene expression studies? Frontiers in Neurogenomics.</p> -</blockquote> - - </TR></TABLE> - </TD> - </TR> - <TR> - <TD align=center bgColor=#ddddff class="solidBorder"> - <!--Start of footer--> - <TABLE width="90%"> - <script language='JavaScript' src='/javascript/footer.js'></script> - <TR> - <TD colspan=3 class="fs12"> - <UL> - - </UL> - </TD> - </TR> - </TABLE> - <!--End of footer--> - </TD> - </TR> -</TABLE> -<!-- /Footer --> -<!-- menu script itself. you should not modify this file --> -<script language="JavaScript" src="/javascript/menu_new.js"></script> -<!-- items structure. menu hierarchy and links are stored there --> -<script language="JavaScript" src="/javascript/menu_items.js"></script> -<!-- files with geometry and styles structures --> -<script language="JavaScript" src="/javascript/menu_tpl.js"></script> -<script language="JavaScript"> - <!--// - // Note where menu initialization block is located in HTML document. - // Don't try to position menu locating menu initialization block in - // some table cell or other HTML element. Always put it before </body> - // each menu gets two parameters (see demo files) - // 1. items structure - // 2. geometry structure - new menu (MENU_ITEMS, MENU_POS); - // make sure files containing definitions for these variables are linked to the document - // if you got some javascript error like "MENU_POS is not defined", then you've made syntax - // error in menu_tpl.js file or that file isn't linked properly. - - // also take a look at stylesheets loaded in header in order to set styles - //--> - -</script> -</BODY> -</HTML> |