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    <title>Genomics</title>
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      <title>Somatic genomics pioneer Quotient signs $2.2B IBD deal with Merck</title>
      <description>
        <![CDATA[For a company founded only four years ago, Quotient Therapeutics Inc. entered its third major deal, this time with Merck & Co. Inc. to find novel drug targets for inflammatory bowel disease (IBD) using its somatic genomics platform technology.]]>
      </description>
      <guid>http://www.bioworld.com/articles/729823</guid>
      <pubDate>Tue, 24 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729823-somatic-genomics-pioneer-quotient-signs-22b-ibd-deal-with-merck</link>
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        <media:title type="plain">Gastrointestinal system with DNA, scientific background</media:title>
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      <title>A fresh look at 1000 Genomes is more detailed, and more panoramic</title>
      <description>
        <![CDATA[The human genome has yielded another round of secrets with the publication of two back-to-back papers in <em>Nature</em> on July 23, 2025. Both studies re-sequenced probands from the open-access 1000 Genomes Project, which was one of the first projects to sequence individuals from diverse populations.]]>
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      <guid>http://www.bioworld.com/articles/722504</guid>
      <pubDate>Thu, 24 Jul 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/722504-a-fresh-look-at-1000-genomes-is-more-detailed-and-more-panoramic</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/1000Genomes-hero-7-23.webp?t=1753283063" type="image/jpeg" medium="image" fileSize="666516">
        <media:title type="plain">Illustration of group of people with chromosomes floating above</media:title>
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    <item>
      <title>A fresh look at 1000 Genomes is more detailed, and more panoramic</title>
      <description>
        <![CDATA[The human genome has yielded another round of secrets with the publication of two back-to-back papers in <em>Nature</em> on July 23, 2025. Both studies re-sequenced probands from the open-access 1000 Genomes Project, which was one of the first projects to sequence individuals from diverse populations. While one paper “goes very deep and tries to reconstruct a few genomes to basically near completion,” the other specifically looked at structural variants in a larger number of genomes. Together, they give new insights into genome variation.]]>
      </description>
      <guid>http://www.bioworld.com/articles/722402</guid>
      <pubDate>Wed, 23 Jul 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/722402-a-fresh-look-at-1000-genomes-is-more-detailed-and-more-panoramic</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/1000Genomes-hero-7-23.webp?t=1753283063" type="image/jpeg" medium="image" fileSize="666516">
        <media:title type="plain">Illustration of group of people with chromosomes floating above</media:title>
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      <title>UK releases three decades of children’s genomic data</title>
      <description>
        <![CDATA[The U.K. has released a huge repository of children’s genomic data after sequencing blood samples from three large cohorts recruited at birth and followed across three decades. The power of the data is amplified by the large volume of longitudinal health information, biological samples and responses to surveys and questionnaires that has been provided by participating families. Before this, large-scale publicly available genome sequences were limited to adult cohorts, and the only childhood genome sequence data was from children with rare diseases.]]>
      </description>
      <guid>http://www.bioworld.com/articles/718040</guid>
      <pubDate>Wed, 05 Mar 2025 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/718040-uk-releases-three-decades-of-childrens-genomic-data</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Pediatric/pediatrics-kids-diversity.webp?t=1745266580" type="image/jpeg" medium="image" fileSize="321837">
        <media:title type="plain">Group of kids, faces huddled together</media:title>
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      <title>Genomic study paves way for multimorbidity treatments</title>
      <description>
        <![CDATA[A large-scale study cross-referencing genomic data from multiple sources with primary care health records has identified genetic overlaps in 72 chronic diseases, opening the way for a more holistic approach to researching, treating and preventing multimorbidity.]]>
      </description>
      <guid>http://www.bioworld.com/articles/717206</guid>
      <pubDate>Mon, 10 Feb 2025 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/717206-genomic-study-paves-way-for-multimorbidity-treatments</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NIH-NHGRI-RNA-Transcripts.webp?t=1722352094" type="image/png" medium="image" fileSize="1072782">
        <media:title type="plain">DNA, RNA concept art.</media:title>
        <media:description type="plain">Credit: Darryl Leja, National Human Genome Research Institute, NIH
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      <title>Study finds genetic factors behind early-onset type 2 diabetes in South Asians</title>
      <description>
        <![CDATA[A U.K. study has uncovered distinctive genetic drivers of type 2 diabetes in South Asians that lead to faster development of complications, the need for earlier insulin replacement therapy and a weaker response to some widely prescribed drugs. That points to the need to refine care pathways. But in addition, the research provides a potent illustration of how the under-representation in genomics databases of people who are not of white European origin can skew results and be a source of discrimination.]]>
      </description>
      <guid>http://www.bioworld.com/articles/715001</guid>
      <pubDate>Tue, 03 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715001-study-finds-genetic-factors-behind-early-onset-type-2-diabetes-in-south-asians</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NIH-NHGRI-DNA-Double-Helix-with-Data.webp?t=1684507472" type="image/png" medium="image" fileSize="495452">
        <media:title type="plain">The DNA double helix overlays a field of ACGTs and binary numbers.</media:title>
        <media:description type="plain">Credit: Jonathan Bailey, National Human Genome Research Institute, NIH
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      <title>Through comparative genomics, becoming tough as nails – or squirrels</title>
      <description>
        <![CDATA[Humans love to think of our species as unique. But on a genetic level, such uniqueness is surprisingly hard to find. And while that may be a blow to the ego, it also means that an evolutionary lens is one way to search for insights into human diseases. Animals are “adapted to use the same genes that you and I have, but in very different ways,” Ashley Zehnder told <em>BioWorld</em>. Zehnder is co-founder and CEO of Fauna Bio Inc., which uses comparative genomics to identify gene networks that underlie disease resistance in different animal species.]]>
      </description>
      <guid>http://www.bioworld.com/articles/705167</guid>
      <pubDate>Tue, 30 Jan 2024 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/705167-through-comparative-genomics-becoming-tough-as-nails-or-squirrels</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/13-lined-ground-squirrel.webp?t=1706654622" type="image/jpeg" medium="image" fileSize="449085">
        <media:title type="plain">13-lined-ground-squirrel.jpg</media:title>
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      <title>In 2023, big projects create ‘satellite maps’ of cell biology</title>
      <description>
        <![CDATA[If we unraveled the DNA of the 46 chromosomes of a single human cell, it would barely measure 2 meters. If we did the same with the rest of the body, if we aligned the 3 billion base pairs of its 5 trillion cells, we could travel the distance from the Earth to the Sun more than 100 times. It seems unreachable. However, that is the unit of knowledge of the large sequencing projects achieved in 2023.]]>
      </description>
      <guid>http://www.bioworld.com/articles/704456</guid>
      <pubDate>Tue, 09 Jan 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/704456-in-2023-big-projects-create-satellite-maps-of-cell-biology</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/Pangenome-reference-hero.webp?t=1703866149" type="image/jpeg" medium="image" fileSize="323844">
        <media:title type="plain">Art concept for pangenome wrapping around the globe</media:title>
        <media:description type="plain">The pangenome reference is a collection of different genomes from which to compare an individual genome sequence. Like a map of the subway system, the pangenome graph has many possible routes for a sequence to take. Credit: Darryl Leja, NHGRI</media:description>
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    </item>
    <item>
      <title>In 2023, big projects create ‘satellite maps’ of cell biology</title>
      <description>
        <![CDATA[If we unraveled the DNA of the 46 chromosomes of a single human cell, it would barely measure 2 meters. If we did the same with the rest of the body, if we aligned the 3 billion base pairs of its 5 trillion cells, we could travel the distance from the Earth to the Sun more than 100 times. It seems unreachable. However, that is the unit of knowledge of the large sequencing projects achieved in 2023. From the generation of the human pangenome to cell-by-cell maps of the brain and kidneys, scientists this year have completed several omics collaborative projects stored in large international databases. Now, what’s the plan?]]>
      </description>
      <guid>http://www.bioworld.com/articles/704380</guid>
      <pubDate>Fri, 05 Jan 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/704380-in-2023-big-projects-create-satellite-maps-of-cell-biology</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/Pangenome-reference-hero.webp?t=1703866149" type="image/jpeg" medium="image" fileSize="323844">
        <media:title type="plain">Art concept for pangenome wrapping around the globe</media:title>
        <media:description type="plain">The pangenome reference is a collection of different genomes from which to compare an individual genome sequence. Like a map of the subway system, the pangenome graph has many possible routes for a sequence to take. Credit: Darryl Leja, NHGRI</media:description>
      </media:content>
    </item>
    <item>
      <title>In 2023, big projects create ‘satellite maps’ of cell biology</title>
      <description>
        <![CDATA[If we unraveled the DNA of the 46 chromosomes of a single human cell, it would barely measure 2 meters. If we did the same with the rest of the body, if we aligned the 3 billion base pairs of its 5 trillion cells, we could travel the distance from the Earth to the Sun more than 100 times. It seems unreachable. However, that is the unit of knowledge of the large sequencing projects achieved in 2023. From the generation of the human pangenome to cell-by-cell maps of the brain and kidneys, scientists this year have completed several omics collaborative projects stored in large international databases. Now, what’s the plan?]]>
      </description>
      <guid>http://www.bioworld.com/articles/704127</guid>
      <pubDate>Fri, 29 Dec 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/704127-in-2023-big-projects-create-satellite-maps-of-cell-biology</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/Pangenome-reference-hero.webp?t=1703866149" type="image/jpeg" medium="image" fileSize="323844">
        <media:title type="plain">Art concept for pangenome wrapping around the globe</media:title>
        <media:description type="plain">The pangenome reference is a collection of different genomes from which to compare an individual genome sequence. Like a map of the subway system, the pangenome graph has many possible routes for a sequence to take. Credit: Darryl Leja, NHGRI</media:description>
      </media:content>
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      <title>‘A trillion in each of us’: Flagship-backed Quotient takes on somatic genomics</title>
      <description>
        <![CDATA[Launching a company based on knowledge that “the fundamental principle that most people hold to be true is off by a trillion” is a rare opportunity, said Jake Rubens, co-founder and president of Quotient Therapeutics Inc., a company that emerged from stealth this week, backed by two years of platform development and a $50 million investment from Flagship Pioneering.]]>
      </description>
      <guid>http://www.bioworld.com/articles/703281</guid>
      <pubDate>Wed, 29 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/703281-a-trillion-in-each-of-us-flagship-backed-quotient-takes-on-somatic-genomics</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Cells-and-DNA-helix.webp?t=1602701583" type="image/png" medium="image" fileSize="424450">
        <media:title type="plain">Cells and DNA helix</media:title>
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    </item>
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      <title>‘A trillion in each of us’: Flagship-backed Quotient takes on somatic genomics</title>
      <description>
        <![CDATA[Launching a company based on knowledge that “the fundamental principle that most people hold to be true is off by a trillion” is a rare opportunity, said Jake Rubens, co-founder and president of Quotient Therapeutics Inc., a company that emerged from stealth this week, backed by two years of platform development and a $50 million investment from Flagship Pioneering.]]>
      </description>
      <guid>http://www.bioworld.com/articles/703218</guid>
      <pubDate>Wed, 22 Nov 2023 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/703218-a-trillion-in-each-of-us-flagship-backed-quotient-takes-on-somatic-genomics</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Cells-and-DNA-helix.webp?t=1602701583" type="image/png" medium="image" fileSize="424450">
        <media:title type="plain">Cells and DNA helix</media:title>
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      <title>Pangenome gives more panoramic view of human diversity</title>
      <description>
        <![CDATA[The human genome, the sequence that represents the DNA of our species, was built with a single individual as a model. This all-in-one standard didn’t include the gene variations that make us different or explain why some people develop certain diseases. Four simultaneous studies from the Human Pangenome Reference Consortium have published a sequence based on 47 individuals, beginning to capture the genetic diversity that defines humans.]]>
      </description>
      <guid>http://www.bioworld.com/articles/696850</guid>
      <pubDate>Wed, 10 May 2023 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/696850-pangenome-gives-more-panoramic-view-of-human-diversity</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/Pangenome-hero.webp?t=1683731828" type="image/jpeg" medium="image" fileSize="166488">
        <media:title type="plain">Illustration showing pangenome graph</media:title>
        <media:description type="plain">The new pangenome reference is a collection of different genomes from which to compare an individual genome sequence. Like a map of the subway system, the pangenome graph has many possible routes for a sequence to take, represented by the different colors. The detouring paths at the top of the image represent single nucleotide variants (SNVs), which are single letter differences. The yellow path that loops around itself and repeats the same nucleotides represents a duplication variant. The pink path that loops counterclockwise and follows the nucleotide sequence backwards represents an inversion variant. At the bottom, the green and dark blue paths miss the C nucleotide in its route and represent a deletion variant. The light blue path, which has extra nucleotides in its route, represents an insertion variant. Credit: Darryl Leja, National Human Genome Research Institute, NIH</media:description>
      </media:content>
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      <title>Parallel sequencing yields genomic secrets of extrachromosomal DNA</title>
      <description>
        <![CDATA[A method for parallel sequencing of single-cell extrachromosomal circular DNA (ecDNA) and full-length mRNA transcriptomes has enabled new insights into the roles of ecDNA in cancer progression, researchers from Charité hospital and the Max Delbrück Center for Molecular Medicine reported in <em>Nature Genetics</em> on May 8, 2023. Circular DNAs are present in at least a third of cancer cells, and their presence correlates with poor prognosis in many cases. They can carry driver genes that have separated themselves from their chromosome of origin, and some research suggests that they serve as “reserve copies” of driver genes. Boundless Bio Inc. is in phase I trials targeting ecDNAs.]]>
      </description>
      <guid>http://www.bioworld.com/articles/696756</guid>
      <pubDate>Mon, 08 May 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/696756-parallel-sequencing-yields-genomic-secrets-of-extrachromosomal-dna</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/ecDNA-hero.webp?t=1683557294" type="image/jpeg" medium="image" fileSize="320532">
        <media:title type="plain">Nuclei and chromosomes of neuroblastoma cells</media:title>
        <media:description type="plain">Nuclei and chromosomes of neuroblastoma cells. DNA rings are colored yellow, turquoise, or magenta. Each color is associated with different cancer genes. Credit: Charité/ Rocío Chamorro González</media:description>
      </media:content>
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      <title>Tracking metastases by gene expression unveils four subtypes of cancer</title>
      <description>
        <![CDATA[Cells that break away from a tumor and colonize other regions of the body express genes that are different from those of the cancer from which they originate. Now, a Baylor College of Medicine study has found that metastases can be classified into four cancer subtypes regardless of the primary cancer. This finding describes which genes are active in each one, making it possible to establish the most appropriate treatments for each patient according to the subtype of metastasis they have developed.]]>
      </description>
      <guid>http://www.bioworld.com/articles/693828</guid>
      <pubDate>Wed, 01 Feb 2023 11:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/693828-tracking-metastases-by-gene-expression-unveils-four-subtypes-of-cancer</link>
    </item>
    <item>
      <title>Blood cells can tell tales about risk of neurological and psychiatric disorders</title>
      <description>
        <![CDATA[A genome-wide association study (GWAS) from The University of Queensland has linked blood cell traits (BCTs) and neurological and psychiatric disorders (NPDs), providing a tool to improve patient treatments or repurposing different drugs. The researchers also found a cause-effect relationship between Parkinson's and platelet distribution width. In their study, published Jan. 25, 2023, in <em>Cell Genomics</em>, the scientists observed the genetic overlap between common NPDs and 29 BCTs, including functional genes, regulatory elements and new genetic correlations linked to hematological data and for these diseases.]]>
      </description>
      <guid>http://www.bioworld.com/articles/693599</guid>
      <pubDate>Wed, 25 Jan 2023 11:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/693599-blood-cells-can-tell-tales-about-risk-of-neurological-and-psychiatric-disorders</link>
    </item>
    <item>
      <title>UCLA biobank takes advantage of LA’s diversity</title>
      <description>
        <![CDATA[Los Angeles is one of the most diverse cities in the U.S. This diversity is evident at University of California, Los Angeles (UCLA), a university that attracts students (37,000) and workers (22,090) from 118 countries. It is enough to go for a walk on campus or its surroundings to believe that one is at a United Nations convention. Researchers at the UCLA ATLAS Community Health Initiative has been capturing that diversity in a genomic biobank whose data will help to understand, anonymously, the genetic basis of certain diseases. With them, scientists will be able to design the best treatments for these patients.]]>
      </description>
      <guid>http://www.bioworld.com/articles/693241</guid>
      <pubDate>Thu, 12 Jan 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/693241-ucla-biobank-takes-advantage-of-las-diversity</link>
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    <item>
      <title>Some male cancer cells inactivate the X chromosome</title>
      <description>
        <![CDATA[X-chromosome inactivation (XCI) is not unique to female cells and may confer some survival advantage to male cancer cells, according to scientists at the Dana-Farber Cancer Institute at Harvard. The noncoding RNA XIST (acronym for X-inactive specific transcript), which in female mammals (of genotype XX) inactivates one of the X chromosomes, preventing the overexpression of the genes of the repeated chromosome from early stages of embryonic development, also acts somatically in some male cancers, compensating for the loss of the entire chromosome. <br><br>“We found that a small percentage of male cancers are expressing XIST, which normally is expressed in female cancers. And the percentage of male cancers that express XIST is variable depending on the cancer type,” Srinivas Viswanathan, researcher in the Department of Medical Oncology at the Dana-Farber Cancer Institute at Harvard and assistant professor of Medicine at Harvard Medical School, told <em>BioWorld</em>.]]>
      </description>
      <guid>http://www.bioworld.com/articles/691484</guid>
      <pubDate>Fri, 11 Nov 2022 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/691484-some-male-cancer-cells-inactivate-the-x-chromosome</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/X-inactivation-hero.webp?t=1668183494" type="image/png" medium="image" fileSize="911737">
        <media:title type="plain">A still from an X inactivation animation</media:title>
        <media:description type="plain">A still from an X Inactivation animation. Credit: Walter and Eliza Hall Institute</media:description>
      </media:content>
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    <item>
      <title>Ten new variants linked to Crohn's disease</title>
      <description>
        <![CDATA[In the largest study to date for Crohn's disease, researchers from the Wellcome Sanger Institute and the Broad Institute of MIT and Harvard identified rare variants of 10 genes associated with this pathology. The researchers sequenced the exomes of 110,000 people, 30,000 patients with Crohn's and 80,000 without this condition, with the participation of a hundred international scientific institutions.]]>
      </description>
      <guid>http://www.bioworld.com/articles/667491</guid>
      <pubDate>Thu, 01 Sep 2022 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/667491-ten-new-variants-linked-to-crohns-disease</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/DNA-gastrointestinal-colon-cancer.webp?t=1635371735" type="image/png" medium="image" fileSize="361682">
        <media:title type="plain">Illustration of DNA, digestive system</media:title>
      </media:content>
    </item>
    <item>
      <title>Telomere to telomere, the human genome is done</title>
      <description>
        <![CDATA[There is a project management joke that the first 90% of a project takes 90% of the time, whereas the last 10% of the project takes the other 90% of the time.]]>
      </description>
      <guid>http://www.bioworld.com/articles/517527</guid>
      <pubDate>Fri, 01 Apr 2022 10:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/517527-telomere-to-telomere-the-human-genome-is-done</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/DNA-NGS-genome-sequencing.webp?t=1588871366" type="image/png" medium="image" fileSize="527937">
        <media:title type="plain">DNA NGS genome sequencing</media:title>
      </media:content>
    </item>
    <item>
      <title>Genetic findings pave way to treatment of lymph disorder</title>
      <description>
        <![CDATA[An international collaboration led by scientists at The University of South Australia, SA Pathology in Adelaide, and the de Duve Institute, University of Louvain, Belgium, has discovered biallelic <em>MDFIC</em> pathogenic variants underlying the severe lymphatic disorder, central conducting lymphatic anomaly (CCLA), in seven people from six separate families.]]>
      </description>
      <guid>http://www.bioworld.com/articles/516699</guid>
      <pubDate>Mon, 07 Mar 2022 10:05:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/516699-genetic-findings-pave-way-to-treatment-of-lymph-disorder</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Lymph-nodes.webp?t=1602705525" type="image/png" medium="image" fileSize="389735">
        <media:title type="plain">Lymph nodes</media:title>
      </media:content>
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      <title>Fabric Genomics AI quickly identifies 90% of rare disease genomic variants</title>
      <description>
        <![CDATA[Fabric Genomics Inc.’s Gem artificial intelligence algorithm plus whole genome and whole exome data detected more than 90% of disease-causing variants in infants with rare diseases, a study in <em>Genome Medicine</em> demonstrated. The full process from blood sample to shortlist of causative variants and likely diseases takes just a matter of hours and the time to interpret whole genomes is condensed to about 15 minutes.]]>
      </description>
      <guid>http://www.bioworld.com/articles/512394</guid>
      <pubDate>Thu, 14 Oct 2021 13:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/512394-fabric-genomics-ai-quickly-identifies-90-of-rare-disease-genomic-variants</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Gene-therapy.webp?t=1588872558" type="image/png" medium="image" fileSize="1586227">
        <media:title type="plain">DNA data illustration</media:title>
      </media:content>
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      <title>Analysis boosts genomics-driven precision medicine</title>
      <description>
        <![CDATA[The most comprehensive international collaborative analysis to date of the impact of variants on gene expression has revealed thousands of previously unknown regulatory genomic regions controlling disease-linked genes, representing a major advance in genomics-driven precision medicine.]]>
      </description>
      <guid>http://www.bioworld.com/articles/511144</guid>
      <pubDate>Tue, 07 Sep 2021 10:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/511144-analysis-boosts-genomics-driven-precision-medicine</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Gene-therapy.webp?t=1588872558" type="image/png" medium="image" fileSize="1586227">
        <media:title type="plain">DNA data illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Diverse cohort expands diabetes genomics</title>
      <description>
        <![CDATA[Data on the prevalence of diabetes in the U.S. show that non-Hispanic white people are least likely to suffer from the disease. Yet to date most genetic studies of the glycemic traits that are used to diagnose and monitor type 2 diabetes and cardiometabolic health have focused on individuals of European ancestry.]]>
      </description>
      <guid>http://www.bioworld.com/articles/507789</guid>
      <pubDate>Thu, 03 Jun 2021 13:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/507789-diverse-cohort-expands-diabetes-genomics</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2021/Jun-2021/Science-diabetes-genomics-6-1.webp?t=1622574227" type="image/png" medium="image" fileSize="512846">
        <media:title type="plain">Child, DNA, genomics illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Diverse cohort expands diabetes genomics</title>
      <description>
        <![CDATA[Data on the prevalence of diabetes in the U.S. show that non-Hispanic white people are least likely to suffer from the disease. Yet to date most genetic studies of the glycemic traits that are used to diagnose and monitor type 2 diabetes and cardiometabolic health have focused on individuals of European ancestry.]]>
      </description>
      <guid>http://www.bioworld.com/articles/507693</guid>
      <pubDate>Tue, 01 Jun 2021 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/507693-diverse-cohort-expands-diabetes-genomics</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2021/Jun-2021/Science-diabetes-genomics-6-1.webp?t=1622574227" type="image/png" medium="image" fileSize="512846">
        <media:title type="plain">Child, DNA, genomics illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Quick-ish cleanup can preserve privacy in functional genomics datasets</title>
      <description>
        <![CDATA[Researchers at Yale University have described what they have called a “data sanitization tool,” enabling them to strip personal identifiers out of functional genomics data while preserving their usefulness for research.]]>
      </description>
      <guid>http://www.bioworld.com/articles/500124</guid>
      <pubDate>Thu, 12 Nov 2020 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/500124-quick-ish-cleanup-can-preserve-privacy-in-functional-genomics-datasets</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2020/Nov-2020/Science-data-privacy-11-12.webp?t=1605212949" type="image/png" medium="image" fileSize="109028">
        <media:title type="plain">Data privacy illustration</media:title>
        <media:description type="plain">Credit: Wendolyn Hill</media:description>
      </media:content>
    </item>
    <item>
      <title>GTEx explores variation in genome bureaucracy</title>
      <description>
        <![CDATA[The Genotype-Tissue Expression (GTEx) project, a multiyear, multi-institutional attempt to catalog how expression quantitative trait loci (eQTL) and splicing quantitative trait loci (sQTL) affect protein levels, reported data from its final phase in 15 papers in the Sept, 10, 2020, online issues of the <em>Science</em> and <em>Cell</em> family of journals, as well as in <em>Genome Biology</em>.]]>
      </description>
      <guid>http://www.bioworld.com/articles/497617</guid>
      <pubDate>Thu, 10 Sep 2020 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/497617-gtex-explores-variation-in-genome-bureaucracy</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2020/Sep-2020/Science-expression-quantitative-trait-loci-9-10.webp?t=1599749138" type="image/png" medium="image" fileSize="381388">
        <media:title type="plain">Expression quantitative trait loci</media:title>
        <media:description type="plain">Sections of the genome, known as expression Quantitative Trait
Loci (eQTL), work to control how genes are turned off and on.
Variants in eQTLs affect how much of a protein a cell will produce.
Credit: Darryl Leja, National Human Genome Research Institute, NIH</media:description>
      </media:content>
    </item>
    <item>
      <title>Data reported from ENCODE phase III</title>
      <description>
        <![CDATA[Researchers from the Encyclopedia of DNA Elements (ENCODE) consortium reported data from the third phase of the project. Phase III data, which were published in more than a dozen papers in <em>Nature </em> and its sister journals on July 29, 2020, consisted of 6,000 experiments performed on around 1,300 samples.]]>
      </description>
      <guid>http://www.bioworld.com/articles/496333</guid>
      <pubDate>Wed, 29 Jul 2020 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/496333-data-reported-from-encode-phase-iii</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2020/Jul-2020/ENCODE-7-29.webp?t=1596063844" type="image/png" medium="image" fileSize="119520">
        <media:title type="plain">ENCODE project illustration</media:title>
        <media:description type="plain">Image credit, above: ENCODE
Animation credit, below: Ernesto Del Aguila III, NHGRI</media:description>
      </media:content>
    </item>
    <item>
      <title>Gnomad identifies rare loss of function variants</title>
      <description>
        <![CDATA[LONDON – A vast new body of genomics research has identified thousands of rare genetic variants that are predicted to cause loss of function in protein coding genes, providing novel in vivo models of human gene inactivation.]]>
      </description>
      <guid>http://www.bioworld.com/articles/435442</guid>
      <pubDate>Fri, 29 May 2020 13:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/435442-gnomad-identifies-rare-loss-of-function-variants</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/gnomAD.webp?t=1617717050" type="image/png" medium="image" fileSize="349175">
        <media:title type="plain">Genome illustration</media:title>
        <media:description type="plain">Credit: Susanna M. Hamilton, Broad Communications</media:description>
      </media:content>
    </item>
    <item>
      <title>Gnomad identifies rare loss of function variants</title>
      <description>
        <![CDATA[LONDON – A vast new body of genomics research has identified thousands of rare genetic variants that are predicted to cause loss of function in protein coding genes, providing novel in vivo models of human gene inactivation.]]>
      </description>
      <guid>http://www.bioworld.com/articles/435375</guid>
      <pubDate>Wed, 27 May 2020 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/435375-gnomad-identifies-rare-loss-of-function-variants</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/gnomAD.webp?t=1617717050" type="image/png" medium="image" fileSize="349175">
        <media:title type="plain">Genome illustration</media:title>
        <media:description type="plain">Credit: Susanna M. Hamilton, Broad Communications</media:description>
      </media:content>
    </item>
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