<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Labgen</title>
	<atom:link href="https://labgen.com.tr/en/feed/" rel="self" type="application/rss+xml" />
	<link>https://labgen.com.tr</link>
	<description></description>
	<lastBuildDate>Wed, 10 Dec 2025 09:21:34 +0000</lastBuildDate>
	<language>en-GB</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=6.9.1</generator>

<image>
	<url>https://labgen.com.tr/wp-content/uploads/2024/04/labgen-fav.png</url>
	<title>Labgen</title>
	<link>https://labgen.com.tr</link>
	<width>32</width>
	<height>32</height>
</image> 
	<item>
		<title>3rd National HematoOncoGenetic Congress</title>
		<link>https://labgen.com.tr/en/3rd-national-hematooncogenetic-congress/</link>
					<comments>https://labgen.com.tr/en/3rd-national-hematooncogenetic-congress/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Wed, 10 Dec 2025 09:21:34 +0000</pubDate>
				<category><![CDATA[News From Us]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4679</guid>

					<description><![CDATA[We have returned from the 3rd National HematoOncoGenetic Congress with International Participation, held on 27–29 November 2025 at the Juju Premier Palace Hotel Antalya, with wonderful memories and valuable scientific exchanges. As the authorized distributor of QIAGEN, it was both an honor and a pleasure for us to attend the congress once again alongside the [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>We have returned from the 3rd National HematoOncoGenetic Congress with International Participation, held on 27–29 November 2025 at the Juju Premier Palace Hotel Antalya, with wonderful memories and valuable scientific exchanges.</p>
<p>As the authorized distributor of QIAGEN, it was both an honor and a pleasure for us to attend the congress once again alongside the QIAGEN team. Throughout the three-day event, we closely followed the latest scientific developments and had the opportunity to present our advanced technology solutions to esteemed professors, specialists, and colleagues.</p>
<p>At the congress, QIAGEN’s QIAcuity Digital PCR technologies attracted significant attention thanks to their outstanding performance in precision and accuracy. In addition, the newly introduced Franklin software, added to QIAGEN’s portfolio through a recent partnership, stood out as one of the key innovations showcased this year.</p>
<p>On 28 November, within the scope of the congress, an insightful satellite symposium titled “QIAGEN Digital Insights” was held, moderated by Assoc. Prof. Ahmet Cevdet Ceylan and presented by Ruth Burton from QIAGEN. The session offered a comprehensive overview of clinical applications and highlighted how the Franklin digital data analytics platform contributes to clinical decision-support processes—providing valuable perspectives for both us and all participants.</p>
<p>The strong interest shown in our booth, the fruitful discussions we held, and the new professional connections we established throughout the event brought great motivation and energy to our entire team. We extend our heartfelt appreciation to the Associatıon of Medical Genetics, the organizing committee, all speakers, the QIAGEN family, and our esteemed professors for their contributions to this meaningful gathering.</p>
<p>We look forward to many more scientific meetings together!</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/3rd-national-hematooncogenetic-congress/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>We Connected with Healthcare Professionals at the 8th National Clinical Microbiology Congress 2025!</title>
		<link>https://labgen.com.tr/en/we-connected-with-healthcare-professionals-at-the-8th-national-clinical-microbiology-congress-2025/</link>
					<comments>https://labgen.com.tr/en/we-connected-with-healthcare-professionals-at-the-8th-national-clinical-microbiology-congress-2025/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Wed, 10 Dec 2025 09:18:08 +0000</pubDate>
				<category><![CDATA[News From Us]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4668</guid>

					<description><![CDATA[This year, we were pleased to take part at the Qiagen booth during this valuable event where the latest scientific developments in clinical microbiology were shared. It was a great opportunity to meet healthcare professionals and industry stakeholders. Throughout the congress, we had the chance to present our innovative solutions, share up-to-date approaches to laboratory [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>This year, we were pleased to take part at the Qiagen booth during this valuable event where the latest scientific developments in clinical microbiology were shared. It was a great opportunity to meet healthcare professionals and industry stakeholders.</p>
<p>Throughout the congress, we had the chance to present our innovative solutions, share up-to-date approaches to laboratory practices, and engage in productive discussions with many centers.</p>
<p>We sincerely thank all participants who visited our booth and showed interest in our work at this event, where we aim to strengthen scientific collaboration and contribute to advancements in diagnostics.</p>
<p>We would also like to thank all institutions and academicians who contributed to the organization, and we look forward to continuing to shape the future of clinical microbiology together.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/we-connected-with-healthcare-professionals-at-the-8th-national-clinical-microbiology-congress-2025/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>34th National Pathology Congress</title>
		<link>https://labgen.com.tr/en/34th-national-pathology-congress/</link>
					<comments>https://labgen.com.tr/en/34th-national-pathology-congress/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Wed, 10 Dec 2025 08:36:28 +0000</pubDate>
				<category><![CDATA[News From Us]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4661</guid>

					<description><![CDATA[Dear Connections, We were delighted to participate in the 34th National Pathology Congress, held on 12–16 November 2025 at Pine Beach Hotel, Antalya, as Qiagen’s authorized distributor and in collaboration with Qiagen. Throughout the congress, we were present at the Qiagen booth, where we had the opportunity to meet esteemed professors and specialists from the [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>Dear Connections,</p>
<p>We were delighted to participate in the 34th National Pathology Congress, held on 12–16 November 2025 at Pine Beach Hotel, Antalya, as Qiagen’s authorized distributor and in collaboration with Qiagen.</p>
<p>Throughout the congress, we were present at the Qiagen booth, where we had the opportunity to meet esteemed professors and specialists from the field, and to share Qiagen’s innovative solutions with participants. We also attended Qiagen’s presentation in the scientific program, gaining deeper insights into the current applications of our product portfolio in pathology, molecular diagnostics, NGS workflows, and bioinformatics analysis processes.</p>
<p>Among the key scientific and technological topics highlighted during the congress were major diagnostic areas such as cytopathology, bone and soft tissue pathology, pulmonary pathology, and uropathology, as well as molecular pathology, NGS applications, genomic instability, biomarker-based approaches, and emerging markers in immunohistochemistry. In addition, sessions on digital pathology, AI-assisted image analytics, deep learning–based decision-support systems, and bioinformatics data analysis and reporting provided highly valuable insights.</p>
<p>As the Labgen team, we conducted one-on-one meetings with visitors, evaluated user experiences and field requirements, and addressed questions particularly related to NGS workflows, bioinformatics data interpretation, and IHC panel optimization. We also attended sessions presented by distinguished experts, gaining numerous new perspectives that will contribute directly to our work.</p>
<p>We sincerely thank the Turkish Federation of Pathology Societies, all speakers, the Qiagen team, and all esteemed professors for this productive organization.</p>
<p>With the knowledge we gained and the new connections we established, we will continue to provide stronger, more up-to-date, and more effective solutions in the field of laboratory diagnostics.</p>
<p>Kind regards,<br />
Labgen</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/34th-national-pathology-congress/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>We Attended an Awareness Event on the Quantiferon TB Gold Plus Test</title>
		<link>https://labgen.com.tr/en/we-attended-an-awareness-event-on-the-quantiferon-tb-gold-plus-test/</link>
					<comments>https://labgen.com.tr/en/we-attended-an-awareness-event-on-the-quantiferon-tb-gold-plus-test/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Wed, 02 Jul 2025 11:29:08 +0000</pubDate>
				<category><![CDATA[News From Us]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4641</guid>

					<description><![CDATA[On March 25, 2025, an important informational meeting was held at Pamukkale University Hospital. Organized to raise awareness about Qiagen’s advanced technology product, the Quantiferon TB Gold Plus test, the event brought together numerous specialist physicians and healthcare professionals from various departments. Representatives from several branches—primarily Adult and Pediatric Infectious Diseases, Dermatology, and Rheumatology—participated in [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>On March 25, 2025, an important informational meeting was held at Pamukkale University Hospital. Organized to raise awareness about Qiagen’s advanced technology product, the Quantiferon TB Gold Plus test, the event brought together numerous specialist physicians and healthcare professionals from various departments.</p>
<p>Representatives from several branches—primarily Adult and Pediatric Infectious Diseases, Dermatology, and Rheumatology—participated in the event. The presentation covered the clinical use of the Quantiferon test, its scientific foundation, application advantages, and result interpretation processes in detail.</p>
<p>The Quantiferon TB Gold Plus test offers a more reliable solution compared to classical methods by providing high specificity and sensitivity in the diagnosis of latent tuberculosis infection.</p>
<p>The main goal of the event was to encourage the more effective use of the test in clinical practice and to build shared awareness among healthcare professionals regarding diagnostic processes.</p>
<p>As Labgen, we will continue to strengthen our collaborations in the healthcare sector and contribute to diagnostic processes with innovative solutions.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/we-attended-an-awareness-event-on-the-quantiferon-tb-gold-plus-test/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>Clinical Variant Analysis with Qiagen Clinical Insight (QCI)</title>
		<link>https://labgen.com.tr/en/clinical-variant-analysis-with-qiagen-clinical-insight-qci/</link>
					<comments>https://labgen.com.tr/en/clinical-variant-analysis-with-qiagen-clinical-insight-qci/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Mon, 03 Mar 2025 07:34:07 +0000</pubDate>
				<category><![CDATA[BIOINFORMATICS SERVICES]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4143</guid>

					<description><![CDATA[The QCI Interpret platform is a software platform developed for clinical genetic testing and biomarker analysis. This tool is designed to assist healthcare professionals in interpreting genetic data, reporting, and clinical decision-making processes. It is commonly used in the evaluation of data related to cancer, hereditary diseases, and other genetic conditions. QCI Interpret provides a [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>The QCI Interpret platform is a software platform developed for clinical genetic testing and biomarker analysis. This tool is designed to assist healthcare professionals in interpreting genetic data, reporting, and clinical decision-making processes. It is commonly used in the evaluation of data related to cancer, hereditary diseases, and other genetic conditions. QCI Interpret provides a detailed analysis of clinical variants and classifies genetic variants according to ACMG (American College of Medical Genetics) guidelines. Clinically significant variants are evaluated in categories such as pathogenicity, benignity, and likely benign. It is highly useful in the fields of oncology, hereditary diseases, and rare diseases with advanced variant interpretation features. In somatic analyses, it provides prognostic evaluations and offers insights into the possible course of diseases. It allows the integration of data obtained from different genetic tests. With a user-friendly interface, it reports genetic test results in an understandable way. It offers tools for identifying specific biomarkers and evaluating their clinical significance. It conducts a comprehensive literature review to provide up-to-date information on genetic variations. It helps develop individualized treatment approaches based on genetic test results.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/clinical-variant-analysis-with-qiagen-clinical-insight-qci/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>NGS (Next-Generation Sequencing) Analysis (Secondary Analysis) with CLC Genomics Workbench</title>
		<link>https://labgen.com.tr/en/ngs-next-generation-sequencing-analysis-secondary-analysis-with-clc-genomics-workbench/</link>
					<comments>https://labgen.com.tr/en/ngs-next-generation-sequencing-analysis-secondary-analysis-with-clc-genomics-workbench/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Mon, 03 Mar 2025 07:34:52 +0000</pubDate>
				<category><![CDATA[BIOINFORMATICS SERVICES]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4145</guid>

					<description><![CDATA[CLC Genomics Workbench is a powerful bioinformatics software platform used for the analysis of genetic and genomic data. It is designed to process large-scale NGS (Next-Generation Sequencing) data, align sequences with high accuracy, and perform analyses with high sensitivity. The platform provides comprehensive data processing tools for genome, transcriptome, metagenome, and epigenome analyses. With its [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>CLC Genomics Workbench is a powerful bioinformatics software platform used for the analysis of genetic and genomic data. It is designed to process large-scale NGS (Next-Generation Sequencing) data, align sequences with high accuracy, and perform analyses with high sensitivity. The platform provides comprehensive data processing tools for genome, transcriptome, metagenome, and epigenome analyses. With its user-friendly interface, it optimizes NGS analyses while enabling the fast and efficient analysis of large datasets. In addition to genomic data, it offers various tools for RNA-Seq, metagenomic analyses, and epigenetic data evaluation. By visually presenting analysis results, it enhances the interpretation and understanding of complex datasets.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/ngs-next-generation-sequencing-analysis-secondary-analysis-with-clc-genomics-workbench/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>Access to and Integration with Robust Clinical Databases</title>
		<link>https://labgen.com.tr/en/access-to-and-integration-with-robust-clinical-databases/</link>
					<comments>https://labgen.com.tr/en/access-to-and-integration-with-robust-clinical-databases/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Mon, 03 Mar 2025 07:35:47 +0000</pubDate>
				<category><![CDATA[BIOINFORMATICS SERVICES]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4147</guid>

					<description><![CDATA[COSMIC (Catalogue of Somatic Mutations in Cancer): A comprehensive database focused on somatic mutations associated with cancer. It serves as a valuable resource, particularly for scientists working in the field of cancer genetics and biology. HGMD (Human Gene Mutation Database): A database that compiles mutations found in human genes and their associations with diseases. It [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>COSMIC (Catalogue of Somatic Mutations in Cancer): A comprehensive database focused on somatic mutations associated with cancer. It serves as a valuable resource, particularly for scientists working in the field of cancer genetics and biology.</p>
<p>HGMD (Human Gene Mutation Database): A database that compiles mutations found in human genes and their associations with diseases. It is a crucial resource for the research, diagnosis, and treatment of genetic disorders. HGMD helps scientists, clinical geneticists, and researchers understand the impact of genetic variations on human health.</p>
<p>HSMD (Human Somatic Mutation Database): A database that collects and analyzes human somatic mutations. It is an essential resource for scientists studying the genetic basis of cancer and other diseases. Somatic mutations occur in body cells and are not inherited, playing a critical role in the development of conditions such as cancer.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/access-to-and-integration-with-robust-clinical-databases/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>Ingenuity Pathway Analysis (IPA)</title>
		<link>https://labgen.com.tr/en/ingenuity-pathway-analysis-ipa/</link>
					<comments>https://labgen.com.tr/en/ingenuity-pathway-analysis-ipa/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Mon, 03 Mar 2025 07:36:27 +0000</pubDate>
				<category><![CDATA[BIOINFORMATICS SERVICES]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4149</guid>

					<description><![CDATA[Ingenuity Pathway Analysis (IPA) is a software used for the analysis and interpretation of biological data. It is particularly utilized in the examination of genetic, protein, and metabolic data. IPA provides an integrated platform to associate data with biological pathways, cellular processes, and diseases. This tool helps researchers analyze datasets, model biological pathways, and understand [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>Ingenuity Pathway Analysis (IPA) is a software used for the analysis and interpretation of biological data. It is particularly utilized in the examination of genetic, protein, and metabolic data. IPA provides an integrated platform to associate data with biological pathways, cellular processes, and diseases. This tool helps researchers analyze datasets, model biological pathways, and understand the roles of specific genes or proteins. Additionally, IPA can be used to identify potential biomarkers and therapeutic targets, making it a crucial tool in omics studies, clinical research, and drug development.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/ingenuity-pathway-analysis-ipa/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>HLA-B27</title>
		<link>https://labgen.com.tr/en/hla-b27-2/</link>
					<comments>https://labgen.com.tr/en/hla-b27-2/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Mon, 03 Mar 2025 08:28:14 +0000</pubDate>
				<category><![CDATA[HLA DISEASE ASSOCIATIONS]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4217</guid>

					<description><![CDATA[HLA-B27 is a genetic marker protein in our body and is associated with immune system-related diseases. The most common diseases linked to the HLA-B27 gene include ankylosing spondylitis, reactive arthritis, psoriatic arthritis, enteropathic arthritis, and uveitis.]]></description>
										<content:encoded><![CDATA[<p>HLA-B27 is a genetic marker protein in our body and is associated with immune system-related diseases. The most common diseases linked to the HLA-B27 gene include ankylosing spondylitis, reactive arthritis, psoriatic arthritis, enteropathic arthritis, and uveitis.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/hla-b27-2/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
		<item>
		<title>HLA-B57</title>
		<link>https://labgen.com.tr/en/hla-b57-2/</link>
					<comments>https://labgen.com.tr/en/hla-b57-2/#respond</comments>
		
		<dc:creator><![CDATA[Master]]></dc:creator>
		<pubDate>Mon, 03 Mar 2025 08:28:30 +0000</pubDate>
				<category><![CDATA[HLA DISEASE ASSOCIATIONS]]></category>
		<guid isPermaLink="false">https://labgen.com.tr/?p=4219</guid>

					<description><![CDATA[It is another genetic marker that affects the immune system. It is particularly focused on its connection with drug reactions and certain infections. Abacavir allergy, autoimmune diseases, and the treatment of chronic viral infections are influenced by this genetic marker.]]></description>
										<content:encoded><![CDATA[<p>It is another genetic marker that affects the immune system. It is particularly focused on its connection with drug reactions and certain infections. Abacavir allergy, autoimmune diseases, and the treatment of chronic viral infections are influenced by this genetic marker.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://labgen.com.tr/en/hla-b57-2/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
	</channel>
</rss>
