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		<title>SEQanswers - Webinar Series</title>
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			<title>SEQanswers - Webinar Series</title>
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			<title>Democratizing Genomic Diagnostics: A New Model for Global Childhood Cancer Care</title>
			<link>https://www.seqanswers.com/forum/site-news/webinar-series/327295-democratizing-genomic-diagnostics-a-new-model-for-global-childhood-cancer-care</link>
			<pubDate>Fri, 08 May 2026 09:42:04 GMT</pubDate>
			<description>Childhood cancers, effectively fatal 60 years ago, are now curable for up to 85% of children with access to contemporary treatments and care....</description>
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<span style="font-size:14px">Childhood cancers, effectively fatal 60 years ago, are now curable for up to 85% of children with access to contemporary treatments and care. However, for the majority of children in resource-limited settings, outcomes remain poor, with global survival rates closer to 20%—representing one of the largest disparities in global health.<br />
<br />
Despite substantial investments to expand access to medicines and care, diagnostic challenges remain a critical barrier. Analyses suggest that a significant proportion of healthcare resources are wasted due to inaccurate or incomplete diagnosis, while efforts to scale conventional diagnostic approaches have faced implementation challenges in low-resource settings.<br />
<br />
<a href="https://event.on24.com/wcc/r/5341131/918F6C41AC684CB36C60BC293E88DEE6?partnerref=seqwebsite" target="_blank">In this webinar</a>, Dr. Nickhill Bhakta will describe how the St. Jude Global-led DARGAN study is developing and evaluating approaches to expand access to high-quality diagnostic testing through a global network. This includes the exploration of Oxford Nanopore sequencing technologies, such as adaptive sampling.<br />
<br />
<i><u>Please note: This is independent, investigator-led research using Oxford Nanopore technology. Oxford Nanopore products are for research use only (RUO)</u></i>.</span><br />
<br />
<span style="font-size:18px"><b>In this webinar, you will learn about<b></b>:</b></span><ul><li><span style="font-size:14px">The potential of whole genome sequencing with adaptive sampling targeted enrichment to consolidate multiple data types—such as structural variation, copy number changes, and methylation signals—within a single workflow.</span></li>
<li><span style="font-size:14px">Insights from multi-site evaluation studies across the St. Jude Global network assessing feasibility, workflow performance, and concordance with existing diagnostic methods.</span></li>
<li><span style="font-size:14px">Considerations for cost, infrastructure, and implementation when evaluating genomic technologies in low- and middle-income countries.</span></li>
</ul><br />
<span style="font-size:18px"><b>Who should attend:</b></span><br />
<br />
<span style="font-size:14px">Cancer researchers<br />
Genomics researchers<br />
Clinical lab directors<br />
Pediatric oncologists</span>  <div align="center"><a href="https://event.on24.com/wcc/r/5341131/918F6C41AC684CB36C60BC293E88DEE6?partnerref=seqwebsite" target="_blank"><b><span style="font-size:18px">Register Here</span></b></a></div>]]></content:encoded>
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