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		<title>SEQanswers - Events / Conferences</title>
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		<description>Relevant events or scientific conferences that may be of interest to the community.  (Mgmt reserves right to limit commercial content without approval.)</description>
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			<title>SEQanswers - Events / Conferences</title>
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			<title>Hands-on NGS Data Analysis Workshops</title>
			<link>https://www.seqanswers.com/forum/events-conferences/327648-hands-on-ngs-data-analysis-workshops</link>
			<pubDate>Mon, 17 Aug 2026 07:31:30 GMT</pubDate>
			<description>Hi everyone, 
 
just a short note for those of you who are working with NGS data and maybe feel that you would like to understand a bit better what...</description>
			<content:encoded><![CDATA[Hi everyone,<br />
<br />
just a short note for those of you who are working with NGS data and maybe feel that you would like to understand a bit better what is actually happening during the analysis.<br />
<br />
At ecSeq we have been teaching practical NGS data analysis courses for quite a few years now, mostly for PhD students, postdocs and researchers from biology or medicine who generate sequencing data themselves, but do not necessarily have a strong bioinformatics background.<br />
<br />
The courses are very hands-on. We work with real sequencing data and commonly used open-source tools, and usually spend quite a lot of time looking at what happens at the individual analysis steps, what can go wrong, and how you can actually decide whether a result makes sense.<br />
<br />
Depending on the workshop, we cover topics such as:<ul><li>NGS data analysis and variant calling</li>
<li>RNA-Seq</li>
<li>Single-cell RNA-Seq</li>
<li>NGS epigenomics</li>
<li>Nextflow and bioinformatics pipeline development</li>
<li>Linux and command-line basics for NGS analysis</li>
</ul><br />
What we try to teach is not just a list of commands that you can copy and run. Especially with NGS data, I think it is much more useful if you understand why a certain step is there, which assumptions are made, what the QC actually tells you, and when you should probably stop and have a closer look at the data.<br />
<br />
Some of the courses start quite basic, so you don't need to be a bioinformatician to participate.<br />
<br />
If this sounds useful for your own work, you can find the current workshops here: <b><a href="https://www.ecseq.com/ngs-workshops" target="_blank">https://www.ecseq.com/ngs-workshops</a></b>]]></content:encoded>
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