<?xml version="1.0" encoding="UTF-8"?><!-- generator="wordpress/1.5.2" -->
<rss version="0.92">
<channel>
	<title>AMB Community</title>
	<link>http://microarraybulletin.com/community</link>
	<description>Interviews and articles highlighting microarray research</description>
	<lastBuildDate>Wed, 11 Jan 2006 00:49:22 +0000</lastBuildDate>
	<docs>http://backend.userland.com/rss092</docs>
	<language>en</language>

	<item>
		<title>Conference Call: David Wong, UCLA</title>
		<description><![CDATA[Listen to the AMB Symposia conference call with Dr. David Wong on the use of the salivary transcriptome as a diagnostic for human disease]]></description>
		<link>http://microarraybulletin.com/community/?p=69</link>
	</item>
	<item>
		<title>Broad Institute Opens HapMap Genotyping and Data Analysis Infrastructure to Researchers</title>
		<description><![CDATA[The Broad Institute  of Harvard and MIT's David Altshuler, Stacey Gabriel and Mark Daly discuss the lessons learned from the HapMap Project]]></description>
		<link>http://microarraybulletin.com/community/?p=35</link>
	</item>
	<item>
		<title>HapMap-tested Genotyping Assays and Microarrays Used for Association Studies</title>
		<description><![CDATA[Baylor's Richard Gibbs talks about genotyping for the HapMap Project and performing other large-scale epilepsy and cancer genome studies]]></description>
		<link>http://microarraybulletin.com/community/?p=31</link>
	</item>
	<item>
		<title>Scientists Create Japan&#8217;s Largest BioBank for Genetic Studies of 47 Common Diseases</title>
		<description><![CDATA[RIKEN's Yusuke Nakamura discusses plans to genotype more than 10,000 individuals]]></description>
		<link>http://microarraybulletin.com/community/?p=32</link>
	</item>
	<item>
		<title>Perlegen Scientists Genotype 4.6 million SNPs in Phase 2 of the HapMap Project Using Array-based Technologies</title>
		<description><![CDATA[Perlegen's David Cox discusses genotyping Phase 2 of the HapMap project and implications for association studies and patient care]]></description>
		<link>http://microarraybulletin.com/community/?p=30</link>
	</item>
	<item>
		<title>British Geneticists Use HapMap in Major Study of Common Diseases</title>
		<description><![CDATA[Cambridge Medical School's John Todd discusses the controls, samples and collaborations needed to find new associations between gene variants and disease]]></description>
		<link>http://microarraybulletin.com/community/?p=33</link>
	</item>
	<item>
		<title>Researchers Combine Linkage Analysis and Whole-Genome Association Studies to Investigate Autism and Alzheimer’s disease</title>
		<description><![CDATA[<!--cut--><!--/cut-->]]></description>
		<link>http://microarraybulletin.com/community/?p=52</link>
	</item>
	<item>
		<title>Brief: Discovering the Genetic Variations Behind Multiple Sclerosis</title>
		<description><![CDATA[<!--cut--><!--/cut-->]]></description>
		<link>http://microarraybulletin.com/community/?p=51</link>
	</item>
	<item>
		<title>Brief: Finding a Common Variant Associated With Increased Risk of Macular Degeneration</title>
		<description><![CDATA[<!--cut--><!--/cut-->]]></description>
		<link>http://microarraybulletin.com/community/?p=50</link>
	</item>
	<item>
		<title>Brief: 100K SNP Scan Helps Finnish Scientists Uncover 700 New Associations in Cardiovascular Disease</title>
		<description><![CDATA[<!--cut--><!--/cut-->]]></description>
		<link>http://microarraybulletin.com/community/?p=49</link>
	</item>
</channel>
</rss>
