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    <title>MSACL</title>
    <description>What&apos;s happening in the clinical lab community including publications in JMSACL and interviews with the Early Career Network.</description>
    <copyright>2021 MSACL</copyright>
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    <pubDate>Tue, 14 Nov 2023 17:00:00 +0000</pubDate>
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      <title>MSACL</title>
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    <itunes:summary>What&apos;s happening in the clinical lab community including publications in JMSACL and interviews with the Early Career Network.</itunes:summary>
    <itunes:author>MSACL</itunes:author>
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    <itunes:keywords>clinical, clinical chemistry, clinical lab, mass spectrometry</itunes:keywords>
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      <itunes:name>MSACL</itunes:name>
      <itunes:email>chris.herold@msacl.org</itunes:email>
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      <title>The Regulatory Landscape of Laboratory Developed Tests (LDT): A Laboratorian Perspective</title>
      <description><![CDATA[The FDA released a proposed LDT rule and stated it will “end its enforcement discretion” of LDTs. Previously, the FDA explored other avenues for regulating LDTs. We will discuss questions relevant to the draft rule and implications to laboratory medicine, including, but not limited to:
- What are possible implications of FDA regulation of LDTs?
- Is the FDA the appropriate mechanism for this LDT oversight?
- What about modernization of CLIA?
- What would be the financial cost?
- What would be the diagnostic cost?
]]></description>
      <pubDate>Tue, 14 Nov 2023 17:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Stephen Master, Carmen Wiley, Melissa Budelier, Dustin Bunch)</author>
      <link>https://msacl.simplecast.com/episodes/the-regulatory-landscape-of-laboratory-developed-tests-ldt-a-laboratorian-perspective-fqZyg_qt</link>
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      <itunes:title>The Regulatory Landscape of Laboratory Developed Tests (LDT): A Laboratorian Perspective</itunes:title>
      <itunes:author>Stephen Master, Carmen Wiley, Melissa Budelier, Dustin Bunch</itunes:author>
      <itunes:duration>00:56:30</itunes:duration>
      <itunes:summary>The FDA released a proposed LDT rule and stated it will “end its enforcement discretion” of LDTs. Previously, the FDA explored other avenues for regulating LDTs. We will discuss questions relevant to the draft rule and implications to laboratory medicine, including, but not limited to:
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- Is the FDA the appropriate mechanism for this LDT oversight?
- What about modernization of CLIA?
- What would be the financial cost?
- What would be the diagnostic cost?</itunes:summary>
      <itunes:subtitle>The FDA released a proposed LDT rule and stated it will “end its enforcement discretion” of LDTs. Previously, the FDA explored other avenues for regulating LDTs. We will discuss questions relevant to the draft rule and implications to laboratory medicine, including, but not limited to:
- What are possible implications of FDA regulation of LDTs?
- Is the FDA the appropriate mechanism for this LDT oversight?
- What about modernization of CLIA?
- What would be the financial cost?
- What would be the diagnostic cost?</itunes:subtitle>
      <itunes:keywords>fda, lab developed test, mass spectrometry, ldt, lab developed tests, clia</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
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      <itunes:episode>19</itunes:episode>
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      <title>MSACL 2023 : A Chat with Jennifer Van Eyk on her Distinguished Contribution Award Lecture</title>
      <description><![CDATA[Dustin Bunch chats with Jennifer Van Eyk on the fine points of her Distinguished Contribution Award lecture from the previous evening. Recorded onsite at MSACL 2023 Monterey in the Exhibit Hall.
]]></description>
      <pubDate>Wed, 5 Apr 2023 16:30:00 +0000</pubDate>
      <author>chris.herold@msacl.org (MSACL)</author>
      <link>https://msacl.simplecast.com/episodes/msacl-2023-a-chat-with-jennifer-van-eyk-on-her-distinguished-contribution-award-lecture-YMOhe2O4</link>
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      <itunes:title>MSACL 2023 : A Chat with Jennifer Van Eyk on her Distinguished Contribution Award Lecture</itunes:title>
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      <itunes:duration>00:12:09</itunes:duration>
      <itunes:summary>Dustin Bunch chats with Jennifer Van Eyk on the fine points of her Distinguished Contribution Award lecture from the previous evening. Recorded onsite at MSACL 2023 Monterey in the Exhibit Hall.</itunes:summary>
      <itunes:subtitle>Dustin Bunch chats with Jennifer Van Eyk on the fine points of her Distinguished Contribution Award lecture from the previous evening. Recorded onsite at MSACL 2023 Monterey in the Exhibit Hall.</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
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      <title>MSACL 2023 : A Chat with Tim Collier on his Michael S Bereman Award Lecture</title>
      <description><![CDATA[Dustin Bunch chats with Tim Collier on some of the nuances of his Michael S Bereman Award for Innovative Clinical Proteomics lecture from the previous afternoon.  Recorded onsite at MSACL 2023 Monterey in the Exhibit Hall.
]]></description>
      <pubDate>Wed, 5 Apr 2023 16:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Tim Collier, Dustin Bunch)</author>
      <link>https://msacl.simplecast.com/episodes/msacl-2023-chat-with-tim-collier-on-his-michael-s-bereman-award-lecture-783h3F9l</link>
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      <itunes:title>MSACL 2023 : A Chat with Tim Collier on his Michael S Bereman Award Lecture</itunes:title>
      <itunes:author>Tim Collier, Dustin Bunch</itunes:author>
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      <itunes:duration>00:11:33</itunes:duration>
      <itunes:summary>Dustin Bunch chats with Tim Collier on some of the nuances of his Michael S Bereman Award for Innovative Clinical Proteomics lecture from the previous afternoon.  Recorded onsite at MSACL 2023 Monterey in the Exhibit Hall.</itunes:summary>
      <itunes:subtitle>Dustin Bunch chats with Tim Collier on some of the nuances of his Michael S Bereman Award for Innovative Clinical Proteomics lecture from the previous afternoon.  Recorded onsite at MSACL 2023 Monterey in the Exhibit Hall.</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
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      <itunes:episode>17</itunes:episode>
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      <title>The MetaProteomics Initiative : The Cornerstone of Comprehensive Molecular Analysis of the Microbiome Ecosystem</title>
      <description><![CDATA[Through connecting genomic and metabolic information, metaproteomics is an essential approach for understanding how microbiomes function in space and time. The international metaproteomics community is delighted to announce the launch of the Metaproteomics Initiative (www.metaproteomics.org), the goal of which is to promote dissemination of metaproteomics fundamentals, advancements, and applications through collaborative networking in microbiome research.
]]></description>
      <pubDate>Thu, 16 Mar 2023 17:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Tim Van Den Bossche, Olgica Trenchevska, Oleg Karaduta)</author>
      <link>https://msacl.simplecast.com/episodes/the-metaproteomics-initiative-the-cornerstone-of-the-comprehensive-molecular-analysis-of-microbiome-ecosystem-oYnc1O4_</link>
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      <itunes:title>The MetaProteomics Initiative : The Cornerstone of Comprehensive Molecular Analysis of the Microbiome Ecosystem</itunes:title>
      <itunes:author>Tim Van Den Bossche, Olgica Trenchevska, Oleg Karaduta</itunes:author>
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      <itunes:duration>00:41:55</itunes:duration>
      <itunes:summary>Through connecting genomic and metabolic information, metaproteomics is an essential approach for understanding how microbiomes function in space and time. The international metaproteomics community is delighted to announce the launch of the Metaproteomics Initiative (www.metaproteomics.org), the goal of which is to promote dissemination of metaproteomics fundamentals, advancements, and applications through collaborative networking in microbiome research.</itunes:summary>
      <itunes:subtitle>Through connecting genomic and metabolic information, metaproteomics is an essential approach for understanding how microbiomes function in space and time. The international metaproteomics community is delighted to announce the launch of the Metaproteomics Initiative (www.metaproteomics.org), the goal of which is to promote dissemination of metaproteomics fundamentals, advancements, and applications through collaborative networking in microbiome research.</itunes:subtitle>
      <itunes:keywords>msacl, metaproteomics, jmsacl, microbiome</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
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      <itunes:episode>16</itunes:episode>
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      <title>Paper Spray Mass Spectrometry in Clinical Application</title>
      <description><![CDATA[An interview with Lindsey Kirkpatrick, DO, PhD and Nicholas Manicke, PhD discussing the technology behind, and development of, Paper Spray technology, as well as its place in the clinical lab. Read the companion article in JMSACL, Development and validation of a paper spray mass spectrometry method for the rapid quantitation of remdesivir and its active metabolite, GS-441524, in human plasma (https://doi.org/10.1016/j.jmsacl.2022.06.001).
]]></description>
      <pubDate>Thu, 15 Dec 2022 00:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Nicholas Manicke, Lindsey Kirkpatrick, Christopher Chouinard, Mahesheema Ali, Dustin Bunch)</author>
      <link>https://msacl.simplecast.com/episodes/paper-spray-mass-spectrometry-in-clinical-application-PJ7ySIF_</link>
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      <itunes:title>Paper Spray Mass Spectrometry in Clinical Application</itunes:title>
      <itunes:author>Nicholas Manicke, Lindsey Kirkpatrick, Christopher Chouinard, Mahesheema Ali, Dustin Bunch</itunes:author>
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      <itunes:duration>00:34:31</itunes:duration>
      <itunes:summary>An interview with Lindsey Kirkpatrick, DO, PhD and Nicholas Manicke, PhD discussing the technology behind, and development of, Paper Spray technology, as well as its place in the clinical lab. Read the companion article in JMSACL, Development and validation of a paper spray mass spectrometry method for the rapid quantitation of remdesivir and its active metabolite, GS-441524, in human plasma (https://doi.org/10.1016/j.jmsacl.2022.06.001).</itunes:summary>
      <itunes:subtitle>An interview with Lindsey Kirkpatrick, DO, PhD and Nicholas Manicke, PhD discussing the technology behind, and development of, Paper Spray technology, as well as its place in the clinical lab. Read the companion article in JMSACL, Development and validation of a paper spray mass spectrometry method for the rapid quantitation of remdesivir and its active metabolite, GS-441524, in human plasma (https://doi.org/10.1016/j.jmsacl.2022.06.001).</itunes:subtitle>
      <itunes:keywords>paper spray, mass spectrometry, dbs, dried blood spots</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
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      <itunes:episode>15</itunes:episode>
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      <title>The triple quadrupole: Innovation, serendipity and persistence</title>
      <description><![CDATA[An interview with Richard Yost, co-developer of the Triple Quadrupole Mass Spectrometer. How it was developed and why. Read the companion article in JMSACL at https://www.sciencedirect.com/science/article/pii/S2667145X22000141
]]></description>
      <pubDate>Wed, 2 Nov 2022 21:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Mahesheema Ali, Christopher Chouinard, Richard Yost)</author>
      <link>https://msacl.simplecast.com/episodes/the-triple-quadrupole-innovation-serendipity-and-persistence-S25FA5vw</link>
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      <itunes:title>The triple quadrupole: Innovation, serendipity and persistence</itunes:title>
      <itunes:author>Mahesheema Ali, Christopher Chouinard, Richard Yost</itunes:author>
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      <itunes:duration>00:42:40</itunes:duration>
      <itunes:summary>An interview with Richard Yost, co-developer of the Triple Quadrupole Mass Spectrometer. How it was developed and why. Read the companion article in JMSACL at https://www.sciencedirect.com/science/article/pii/S2667145X22000141</itunes:summary>
      <itunes:subtitle>An interview with Richard Yost, co-developer of the Triple Quadrupole Mass Spectrometer. How it was developed and why. Read the companion article in JMSACL at https://www.sciencedirect.com/science/article/pii/S2667145X22000141</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
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      <itunes:episode>14</itunes:episode>
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      <title>JMSACL Journal Club : Supervised Machine Learning for Mass Spectrometry Data Analysis: Experts&apos; Opinion</title>
      <description><![CDATA[<p>We will be talking with Thomas Durant and Edward Lee about recent advances in machine learning (ML) for mass spectrometry (MS) data analysis. The primary focus will be the alignment of these two fields (ML and MS) and how this offers a promising synergy that can be used to optimize workflows, improve result quality, and enhance our understanding of high-dimensional datasets, as well as their inherent relationship with disease biology. We will also dig deeper to understand a basic overview of ML and an ML-based experiment. Overall, we will have a opportunity go through the fundamental principles of supervised ML, outline the steps that are classically involved in an ML-based experiment, and discuss the purpose of good ML practice in the context of a binary MS classification problem.</p>
]]></description>
      <pubDate>Tue, 1 Mar 2022 18:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Dustin Bunch, Pankaj Dwivedi, Thomas Durant, Edward Lee)</author>
      <link>https://msacl.simplecast.com/episodes/jmsacl-journal-club-supervised-machine-learning-for-mass-spectrometry-data-analysis-experts-opinion-aRyYghML</link>
      <content:encoded><![CDATA[<p>We will be talking with Thomas Durant and Edward Lee about recent advances in machine learning (ML) for mass spectrometry (MS) data analysis. The primary focus will be the alignment of these two fields (ML and MS) and how this offers a promising synergy that can be used to optimize workflows, improve result quality, and enhance our understanding of high-dimensional datasets, as well as their inherent relationship with disease biology. We will also dig deeper to understand a basic overview of ML and an ML-based experiment. Overall, we will have a opportunity go through the fundamental principles of supervised ML, outline the steps that are classically involved in an ML-based experiment, and discuss the purpose of good ML practice in the context of a binary MS classification problem.</p>
]]></content:encoded>
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      <itunes:title>JMSACL Journal Club : Supervised Machine Learning for Mass Spectrometry Data Analysis: Experts&apos; Opinion</itunes:title>
      <itunes:author>Dustin Bunch, Pankaj Dwivedi, Thomas Durant, Edward Lee</itunes:author>
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      <itunes:duration>00:58:57</itunes:duration>
      <itunes:summary>A discussion with Thomas Durant and Edward Lee about recent advances in machine learning (ML) for mass spectrometry (MS) data analysis.</itunes:summary>
      <itunes:subtitle>A discussion with Thomas Durant and Edward Lee about recent advances in machine learning (ML) for mass spectrometry (MS) data analysis.</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
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      <itunes:episode>13</itunes:episode>
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      <title>Fireside Chat with Christopher Rose on Single Cell Proteomics</title>
      <description><![CDATA[Christopher Rose shares his thoughts on single cell proteomics. 
]]></description>
      <pubDate>Wed, 29 Sep 2021 17:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Christopher Rose, Pankaj Dwivedi, Oleg Karaduta)</author>
      <link>https://msacl.simplecast.com/episodes/fireside-chat-with-chris-rose-on-single-cell-proteomics-gh3jR7pu</link>
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      <itunes:title>Fireside Chat with Christopher Rose on Single Cell Proteomics</itunes:title>
      <itunes:author>Christopher Rose, Pankaj Dwivedi, Oleg Karaduta</itunes:author>
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      <itunes:duration>01:03:07</itunes:duration>
      <itunes:summary>Christopher Rose shares his thoughts on single cell proteomics. </itunes:summary>
      <itunes:subtitle>Christopher Rose shares his thoughts on single cell proteomics. </itunes:subtitle>
      <itunes:keywords>mass spectrometry, proteomics, single cell proteomics</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
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      <itunes:episode>12</itunes:episode>
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      <title>JMSACL Journal Club : Understanding X-Chromosome Deletion Disorder using metabolomics and lipidomics</title>
      <description><![CDATA[<p>X linked disorders are considerably rare and research analysing human samples is under-represented. Research undertaken in this study used neural progenitor cells from an afflicted patient to begin exploring this rare disorder. While most experimental work focuses on the neurodevelopmental impacts of X-chromosome associated diseases, this work demonstrates that they should also be considered metabolic disorders owing to their perturbations on metabolite and lipid biochemistry. This work aims to use mass spectrometry to improve our understanding of these conditions and guide novel interventions by characterizing disease associated metabolic alterations.</p>
]]></description>
      <pubDate>Fri, 20 Aug 2021 05:26:04 +0000</pubDate>
      <author>chris.herold@msacl.org (Pankaj Dwivedi, Hoda Safari Yazd, Timothy Garrett, Oleg Karaduta)</author>
      <link>https://msacl.simplecast.com/episodes/jmsacl-journal-club-understanding-x-chromosome-deletion-disorder-using-metabolomics-and-lipidomics-7ufmijyq-irPZlCQf</link>
      <content:encoded><![CDATA[<p>X linked disorders are considerably rare and research analysing human samples is under-represented. Research undertaken in this study used neural progenitor cells from an afflicted patient to begin exploring this rare disorder. While most experimental work focuses on the neurodevelopmental impacts of X-chromosome associated diseases, this work demonstrates that they should also be considered metabolic disorders owing to their perturbations on metabolite and lipid biochemistry. This work aims to use mass spectrometry to improve our understanding of these conditions and guide novel interventions by characterizing disease associated metabolic alterations.</p>
]]></content:encoded>
      <enclosure length="56020598" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/cba20d2a-f7a8-4a95-bb50-c5720c8ffb5b/audio/fd21d6f3-9bbf-4e35-a599-e4db00a8354d/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>JMSACL Journal Club : Understanding X-Chromosome Deletion Disorder using metabolomics and lipidomics</itunes:title>
      <itunes:author>Pankaj Dwivedi, Hoda Safari Yazd, Timothy Garrett, Oleg Karaduta</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/6f837757-a040-4769-a283-b0f05a082543/3000x3000/jmsacl-journal-club-icon.jpg?aid=rss_feed"/>
      <itunes:duration>01:09:22</itunes:duration>
      <itunes:summary>Hoda Safari Yadz and Tim Garrett, from the Garrett lab in Florida, join us  for a presentation and discussion of their work on the metabolomic and lipidomic characterization of an X-chromosome deletion disorder in neural progenitor cells, hosted by the JMSACL podcast group.</itunes:summary>
      <itunes:subtitle>Hoda Safari Yadz and Tim Garrett, from the Garrett lab in Florida, join us  for a presentation and discussion of their work on the metabolomic and lipidomic characterization of an X-chromosome deletion disorder in neural progenitor cells, hosted by the JMSACL podcast group.</itunes:subtitle>
      <itunes:keywords>jmsacl, journal club</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>11</itunes:episode>
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    <item>
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      <title>Novel Techniques using Silicon (in silico) and Gold to Improve Imaging Results</title>
      <description><![CDATA[<p><strong>Untargeted small molecule machine learning for MSI</strong></p><p>Cameron Shedlock (until 14:00)</p><p>Mass spectrometry imaging returns large dimensionally complex datasets. Traditional analysis in imaging utilizes a mindset focused on target molecule identification that parses data with a narrow view of molecular exploration. These data analysis methods are specifically focused on exploring differences between a traditional organic acid matrix when compared to using nanoparticles for MSI, which results in very different ionization of small molecules. Analysis methods have taken a shotgun approach using both supervised and unsupervised machine learning to reveal critical trends in MSI datasets. A workflow is being prepared which enables select regions of interest to be compared using powerful machine learning algorithms to offer a holistic approach to data analysis and class comparison.</p><p><strong>Mass spectrometry imaging using gold nanoparticles</strong></p><p>Kate Stumpo, PhD</p><p>Mass spectrometry imaging (MSI) is a powerful analytical method for the simultaneous analysis of hundreds of compounds within a biological sample. Despite the broad applicability of this technique, there is a critical need for advancements in methods for small molecule detection. Some molecular classes of small molecules are more difficult than others to ionize, e.g., neurotransmitters (NTs). The chemical structure of NTs (i.e., primary, secondary, and tertiary amines) affects ionization and has been a noted difficulty in the literature. In order to achieve detection of NTs using MSI, strategies must focus on either changing the chemistry of target molecules to aid in detection or focus on new methods of ionization. This presentation will introduce a new method of ionization, using gold nanoparticles (AuNPs), and the bigger picture of NPs for MSI.</p><p> </p><p> </p>
]]></description>
      <pubDate>Thu, 29 Apr 2021 16:30:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Kate Stumpo, Cameron Shedlock)</author>
      <link>https://msacl.simplecast.com/episodes/novel-techniques-using-silicon-in-silico-and-gold-to-improve-imaging-results-YGCkCYbj</link>
      <content:encoded><![CDATA[<p><strong>Untargeted small molecule machine learning for MSI</strong></p><p>Cameron Shedlock (until 14:00)</p><p>Mass spectrometry imaging returns large dimensionally complex datasets. Traditional analysis in imaging utilizes a mindset focused on target molecule identification that parses data with a narrow view of molecular exploration. These data analysis methods are specifically focused on exploring differences between a traditional organic acid matrix when compared to using nanoparticles for MSI, which results in very different ionization of small molecules. Analysis methods have taken a shotgun approach using both supervised and unsupervised machine learning to reveal critical trends in MSI datasets. A workflow is being prepared which enables select regions of interest to be compared using powerful machine learning algorithms to offer a holistic approach to data analysis and class comparison.</p><p><strong>Mass spectrometry imaging using gold nanoparticles</strong></p><p>Kate Stumpo, PhD</p><p>Mass spectrometry imaging (MSI) is a powerful analytical method for the simultaneous analysis of hundreds of compounds within a biological sample. Despite the broad applicability of this technique, there is a critical need for advancements in methods for small molecule detection. Some molecular classes of small molecules are more difficult than others to ionize, e.g., neurotransmitters (NTs). The chemical structure of NTs (i.e., primary, secondary, and tertiary amines) affects ionization and has been a noted difficulty in the literature. In order to achieve detection of NTs using MSI, strategies must focus on either changing the chemistry of target molecules to aid in detection or focus on new methods of ionization. This presentation will introduce a new method of ionization, using gold nanoparticles (AuNPs), and the bigger picture of NPs for MSI.</p><p> </p><p> </p>
]]></content:encoded>
      <enclosure length="59328885" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/f66f706d-490e-47fc-8882-dff1d4259d49/audio/8421a3cb-f3d7-4fcf-b9a0-33d3f36a9ec1/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>Novel Techniques using Silicon (in silico) and Gold to Improve Imaging Results</itunes:title>
      <itunes:author>Kate Stumpo, Cameron Shedlock</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/bb045c89-e1e9-42c7-a466-c88371216ebb/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:01:48</itunes:duration>
      <itunes:summary>This Mentee/Mentor Scientific Session is a joint presentation that will explore techniques for improving imaging analysis of small molecules, with a focus on neurotransmitters, using data science, and gold (and silver) nanoparticles.</itunes:summary>
      <itunes:subtitle>This Mentee/Mentor Scientific Session is a joint presentation that will explore techniques for improving imaging analysis of small molecules, with a focus on neurotransmitters, using data science, and gold (and silver) nanoparticles.</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>10</itunes:episode>
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      <title>JMSACL Journal Club with Benjamin Owusu</title>
      <description><![CDATA[A presentation and discussion with Dr.  Owusu on his recently published paper in JMSACL entitled Development and validation of a novel LC-MS/MS assay for C-peptide in human serum.
]]></description>
      <pubDate>Fri, 23 Apr 2021 17:03:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Benjamin Owusu, Oleg Karaduta, Dustin Bunch)</author>
      <link>https://msacl.simplecast.com/episodes/jmsacl-journal-club-benjamin-owusu-_ePTZw2t</link>
      <enclosure length="56968399" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/ca0522ab-a0f2-42ea-aac7-c12066bddf49/audio/318d0ccb-d806-4388-b18b-d949922d7dfb/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>JMSACL Journal Club with Benjamin Owusu</itunes:title>
      <itunes:author>Benjamin Owusu, Oleg Karaduta, Dustin Bunch</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/18c09c8d-5eed-4ab1-81b1-3fa9af3ced7e/3000x3000/jmsacl-journal-club-icon.jpg?aid=rss_feed"/>
      <itunes:duration>00:59:21</itunes:duration>
      <itunes:summary>A presentation and discussion with Dr.  Owusu on his recently published paper in JMSACL entitled Development and validation of a novel LC-MS/MS assay for C-peptide in human serum.</itunes:summary>
      <itunes:subtitle>A presentation and discussion with Dr.  Owusu on his recently published paper in JMSACL entitled Development and validation of a novel LC-MS/MS assay for C-peptide in human serum.</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>6</itunes:episode>
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      <title>Electrochemical Strategies in ESI-MS for Lipid Analysis</title>
      <description><![CDATA[<p>Lipids play a vital role in maintaining cellular functions. Altered lipid metabolism is currently considered a hallmark of many diseases, which highlights the importance of the characterization of lipid composition in understanding, diagnosing, and treating pathologies. Discrimination of isomeric species is challenging in lipidomics. In this talk, I will introduce the microdroplet electrochemical methods capable of resolving different types of isomers commonly encountered in lipid samples using electrospray ionization mass spectrometry. The methods take advantage of the voltage-controlled and dramatically accelerated electrochemical derivatization of lipid isomers in microdroplets to achieve structural elucidation. Applications of the electrochemical mass spectrometry methods in real sample analysis will also be included.</p>
]]></description>
      <pubDate>Thu, 22 Apr 2021 07:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Xin Yan)</author>
      <link>https://msacl.simplecast.com/episodes/electrochemical-strategies-in-esi-ms-for-lipid-analysis-go5c2sJb</link>
      <content:encoded><![CDATA[<p>Lipids play a vital role in maintaining cellular functions. Altered lipid metabolism is currently considered a hallmark of many diseases, which highlights the importance of the characterization of lipid composition in understanding, diagnosing, and treating pathologies. Discrimination of isomeric species is challenging in lipidomics. In this talk, I will introduce the microdroplet electrochemical methods capable of resolving different types of isomers commonly encountered in lipid samples using electrospray ionization mass spectrometry. The methods take advantage of the voltage-controlled and dramatically accelerated electrochemical derivatization of lipid isomers in microdroplets to achieve structural elucidation. Applications of the electrochemical mass spectrometry methods in real sample analysis will also be included.</p>
]]></content:encoded>
      <enclosure length="70689349" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/62ca0a8f-cfaf-4c1d-b727-6aeeb8977879/audio/b3ce75f4-4d41-4e3d-8587-089eaa98a0ac/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>Electrochemical Strategies in ESI-MS for Lipid Analysis</itunes:title>
      <itunes:author>Xin Yan</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/c9f4cef1-6dda-4280-8ffc-f0af90750fca/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:13:38</itunes:duration>
      <itunes:summary>An introduction of microdroplet electrochemical methods capable of resolving different types of isomers commonly encountered in lipid samples using electrospray ionization mass spectrometry. </itunes:summary>
      <itunes:subtitle>An introduction of microdroplet electrochemical methods capable of resolving different types of isomers commonly encountered in lipid samples using electrospray ionization mass spectrometry. </itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>8</itunes:episode>
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      <title>Reference data-driven metabolomics and application to nutrition research</title>
      <description><![CDATA[<p>Surveying the food-associated compounds detected in clinical samples, we can differentiate patients with specific diet types, such as predominantly animal protein- versus plant-based diet. In addition, we can identify specific foods associated with clinical outcomes in disease cohorts. With its broad applications, we envision this approach becoming invaluable in nutrition research as well as many other fields once additional reference datasets become available.</p>
]]></description>
      <pubDate>Tue, 20 Apr 2021 17:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Kiana West, Peter Dorrestein)</author>
      <link>https://msacl.simplecast.com/episodes/reference-data-driven-metabolomics-and-application-to-nutrition-research-v_mcqhTx</link>
      <content:encoded><![CDATA[<p>Surveying the food-associated compounds detected in clinical samples, we can differentiate patients with specific diet types, such as predominantly animal protein- versus plant-based diet. In addition, we can identify specific foods associated with clinical outcomes in disease cohorts. With its broad applications, we envision this approach becoming invaluable in nutrition research as well as many other fields once additional reference datasets become available.</p>
]]></content:encoded>
      <enclosure length="75293169" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/52f2fa1f-3d87-4b94-8a2c-c60a28a08ba3/audio/2cb8dcd8-ea95-438d-8447-1b6bea6c27dc/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>Reference data-driven metabolomics and application to nutrition research</itunes:title>
      <itunes:author>Kiana West, Peter Dorrestein</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/a3cb0400-7d97-4598-b238-9ee3af0f5620/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:18:25</itunes:duration>
      <itunes:summary>Untargeted metabolomics experiments suffer from large proportions of unannotated molecules. Using a reference data-driven approach, we increase the spectral annotation rate by assigning potential sources to molecular features. We have applied this approach using a food reference database to generate diet readouts from clinical samples. </itunes:summary>
      <itunes:subtitle>Untargeted metabolomics experiments suffer from large proportions of unannotated molecules. Using a reference data-driven approach, we increase the spectral annotation rate by assigning potential sources to molecular features. We have applied this approach using a food reference database to generate diet readouts from clinical samples. </itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>9</itunes:episode>
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      <title>Empirically tracking the exposure of human plasma &amp; serum samples to thawed conditions</title>
      <description><![CDATA[<p>This presentation will described the concept, methodology, validation and performance characteristics of a 10-µL, dilute-and-shoot, intact-protein mass spectrometric assay of albumin proteoforms called “Delta-S-Cys-Albumin” that serves as an endogenous marker of P/S exposure to thawed conditions based on the inexorable ex vivo S-cysteinylation (oxidizability) of albumin. The multi-reaction chemical mechanism that drives changes in albumin S-cysteinylation is known and the rate law for it was established and accurately modeled in P/S—enabling back-calculation of the time at which unknown P/S specimens have been exposed to the equivalent of room temperature. Results from blind challenges and two unanticipated case studies that revealed unexpected integrity problems in sets of nominally pristine P/S samples will be presented.</p>
]]></description>
      <pubDate>Tue, 6 Apr 2021 17:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Chad Borges)</author>
      <link>https://msacl.simplecast.com/episodes/empirically-tracking-the-exposure-of-human-plasma-serum-samples-to-thawed-conditions-EaYTuB6H</link>
      <content:encoded><![CDATA[<p>This presentation will described the concept, methodology, validation and performance characteristics of a 10-µL, dilute-and-shoot, intact-protein mass spectrometric assay of albumin proteoforms called “Delta-S-Cys-Albumin” that serves as an endogenous marker of P/S exposure to thawed conditions based on the inexorable ex vivo S-cysteinylation (oxidizability) of albumin. The multi-reaction chemical mechanism that drives changes in albumin S-cysteinylation is known and the rate law for it was established and accurately modeled in P/S—enabling back-calculation of the time at which unknown P/S specimens have been exposed to the equivalent of room temperature. Results from blind challenges and two unanticipated case studies that revealed unexpected integrity problems in sets of nominally pristine P/S samples will be presented.</p>
]]></content:encoded>
      <enclosure length="73644248" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/856e0ea7-7507-43de-b992-49d0d0d264d7/audio/635a36ce-7cf3-4e6c-8e14-239295bcf400/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>Empirically tracking the exposure of human plasma &amp; serum samples to thawed conditions</itunes:title>
      <itunes:author>Chad Borges</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/e4d7d0c2-c74d-4043-9c2e-eae0a8d2faf0/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:16:42</itunes:duration>
      <itunes:summary>Exposure of blood plasma/serum (P/S) to thawed conditions (&gt; -30 °C) can produce biomolecular changes that skew measurements of biomarkers within archived patient samples, potentially rendering them unfit for molecular analysis.  Since freeze-thaw histories are often poorly documented, objective methods for assessing molecular fitness prior to analysis are needed.</itunes:summary>
      <itunes:subtitle>Exposure of blood plasma/serum (P/S) to thawed conditions (&gt; -30 °C) can produce biomolecular changes that skew measurements of biomarkers within archived patient samples, potentially rendering them unfit for molecular analysis.  Since freeze-thaw histories are often poorly documented, objective methods for assessing molecular fitness prior to analysis are needed.</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>7</itunes:episode>
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      <title>Getting going with MS (4) : Josh attempts method validation</title>
      <description><![CDATA[<p>This session will outline the studies conducted and planned in order to complete validation of a mass spectrometry method in a CAP-accredited, clinical laboratory. While accuracy and precision and reportable range will be addressed, particular attention will be paid to the additional validation studies that should be conducted (matrix effect, injector stability, interferences, etc).</p>
]]></description>
      <pubDate>Tue, 9 Mar 2021 18:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (MSACL)</author>
      <link>https://msacl.simplecast.com/episodes/getting-going-with-ms-4-josh-attempts-method-validation-S_JvqF0c</link>
      <content:encoded><![CDATA[<p>This session will outline the studies conducted and planned in order to complete validation of a mass spectrometry method in a CAP-accredited, clinical laboratory. While accuracy and precision and reportable range will be addressed, particular attention will be paid to the additional validation studies that should be conducted (matrix effect, injector stability, interferences, etc).</p>
]]></content:encoded>
      <enclosure length="98389114" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/a0d7c083-bc3c-470b-8194-bc0f6b36f8eb/audio/143be7c5-3732-416f-9477-4069f4b44deb/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>Getting going with MS (4) : Josh attempts method validation</itunes:title>
      <itunes:author>MSACL</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/6a2b89ee-d826-4aed-b93d-efce1612ed00/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:42:29</itunes:duration>
      <itunes:summary>In the thrilling conclusion of this four part series, Josh encounters issues with his vacuum manifold, decides to forgo sample preparation, and attempts to validate a dilute-and-shoot mass spectrometry method. Problems are encountered.</itunes:summary>
      <itunes:subtitle>In the thrilling conclusion of this four part series, Josh encounters issues with his vacuum manifold, decides to forgo sample preparation, and attempts to validate a dilute-and-shoot mass spectrometry method. Problems are encountered.</itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>5</itunes:episode>
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      <title>Getting going with MS (3) : Josh analyzes peaks</title>
      <description><![CDATA[<p>Unlike conventional immunoassays which provide simple (and often incorrect!) results, mass spectrometers provide a plethora of data for every peak- qualifier ions, internal standard areas, retention times, peak shapes, etc. This data, often termed metadata, can help clinical laboratories evaluate their peaks to ensure that they are reporting accurate results. Unfortunately, the process of evaluating this metadata can be a doubting challenge. This session will discover our efforts to move ahead with implementing manageable processes for evaluating the metadata necessary to ensure accurate results.</p><p>At the conclusion of this talk, participants should be able to…</p><p>1. Ask questions related to their own efforts to implement monitoring/assessing metadata</p><p>2. List the metadata that must be evaluated to ensure accurate results</p><p>3. Prepare quality assurance metrics for their laboratories utilizing metadata</p>
]]></description>
      <pubDate>Thu, 11 Feb 2021 16:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Min Yu, Joshua Hayden)</author>
      <link>https://msacl.simplecast.com/episodes/getting-going-with-ms-josh-analyzes-peaks-9lM1wJ4p</link>
      <content:encoded><![CDATA[<p>Unlike conventional immunoassays which provide simple (and often incorrect!) results, mass spectrometers provide a plethora of data for every peak- qualifier ions, internal standard areas, retention times, peak shapes, etc. This data, often termed metadata, can help clinical laboratories evaluate their peaks to ensure that they are reporting accurate results. Unfortunately, the process of evaluating this metadata can be a doubting challenge. This session will discover our efforts to move ahead with implementing manageable processes for evaluating the metadata necessary to ensure accurate results.</p><p>At the conclusion of this talk, participants should be able to…</p><p>1. Ask questions related to their own efforts to implement monitoring/assessing metadata</p><p>2. List the metadata that must be evaluated to ensure accurate results</p><p>3. Prepare quality assurance metrics for their laboratories utilizing metadata</p>
]]></content:encoded>
      <enclosure length="93603072" type="audio/mpeg" url="https://cdn.simplecast.com/audio/6e3e4a47-d78a-40c7-b76c-eb371af633a1/episodes/171083b9-1399-4606-bdff-8eaa68de5228/audio/0ce96d2a-6f07-457a-9841-aff4a2e2633f/default_tc.mp3?aid=rss_feed&amp;feed=uPqspfpg"/>
      <itunes:title>Getting going with MS (3) : Josh analyzes peaks</itunes:title>
      <itunes:author>Min Yu, Joshua Hayden</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/ef7aef73-bc6d-45cf-bc66-e2b7177d91d1/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:37:30</itunes:duration>
      <itunes:summary>Continuing on with mass spectrometry misadventures, this session will discuss our efforts to begin analyzing and evaluating mass spectrometry data. </itunes:summary>
      <itunes:subtitle>Continuing on with mass spectrometry misadventures, this session will discuss our efforts to begin analyzing and evaluating mass spectrometry data. </itunes:subtitle>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>4</itunes:episode>
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      <title>Getting going with MS (2) : Josh learns chromatography</title>
      <description><![CDATA[<p>What do we want? Good chromatography! How do we get it? We don’t know! Columns, maybe?</p><p>Good chromatography is essential to any LC-MS/MS method. Setting it up is often one of the earlier steps in developing a new method. While it can be an iterative process, setting up good chromatographic conditions at the start can set you up for success later on. This podcast will discuss our laboratories efforts to setup chromatographic conditions for the analysis of ethyl-glucuronide and buprenorphine (plus metabolites). We will present what we tried, why it seemed like it a good/bad idea, and along the way talk through some basic chromatography concepts. The goal is for attendees to be more informed when they approach setting up their own chromatographic methods.</p><p>This session is the second in a 4 part series in which Dr. Hayden will invite attendees to witness in real time his journey bringing mass spec testing to a clinical lab. During these interactive sessions, attendees will be encouraged to help troubleshoot, and offer advice as desired.</p><p>You can watch the recording of the first session: "Getting going with mass spectrometry: Josh installs a mass spectrometer".</p><p>Subsequent sessions anticipated include:</p><p>Part 3. Getting going with mass spectrometry: Josh tries to do sample preparation</p><p>Part 4. Getting going with mass spectrometry: Josh analyzes peaks</p>
]]></description>
      <pubDate>Thu, 7 Jan 2021 18:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Chris Herold, Adam Rosebrock, Joshua Hayden, Amber Herold, Susan Abbatiello)</author>
      <link>https://msacl.simplecast.com/episodes/getting-going-with-mass-spectrometry-josh-learns-chromatography-_t3QxvGq</link>
      <content:encoded><![CDATA[<p>What do we want? Good chromatography! How do we get it? We don’t know! Columns, maybe?</p><p>Good chromatography is essential to any LC-MS/MS method. Setting it up is often one of the earlier steps in developing a new method. While it can be an iterative process, setting up good chromatographic conditions at the start can set you up for success later on. This podcast will discuss our laboratories efforts to setup chromatographic conditions for the analysis of ethyl-glucuronide and buprenorphine (plus metabolites). We will present what we tried, why it seemed like it a good/bad idea, and along the way talk through some basic chromatography concepts. The goal is for attendees to be more informed when they approach setting up their own chromatographic methods.</p><p>This session is the second in a 4 part series in which Dr. Hayden will invite attendees to witness in real time his journey bringing mass spec testing to a clinical lab. During these interactive sessions, attendees will be encouraged to help troubleshoot, and offer advice as desired.</p><p>You can watch the recording of the first session: "Getting going with mass spectrometry: Josh installs a mass spectrometer".</p><p>Subsequent sessions anticipated include:</p><p>Part 3. Getting going with mass spectrometry: Josh tries to do sample preparation</p><p>Part 4. Getting going with mass spectrometry: Josh analyzes peaks</p>
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      <itunes:title>Getting going with MS (2) : Josh learns chromatography</itunes:title>
      <itunes:author>Chris Herold, Adam Rosebrock, Joshua Hayden, Amber Herold, Susan Abbatiello</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/993801f1-ed99-48bc-9153-dd8c18d2f543/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:37:20</itunes:duration>
      <itunes:summary>Good chromatography is essential to any LC-MS/MS method. Setting it up is often one of the earlier steps in developing a new method. Setting up good chromatographic conditions at the start can set you up for success later on. This podcast will discuss our labs efforts to setup chromatographic conditions for the analysis of ethyl-glucuronide and buprenorphine (plus metabolites).</itunes:summary>
      <itunes:subtitle>Good chromatography is essential to any LC-MS/MS method. Setting it up is often one of the earlier steps in developing a new method. Setting up good chromatographic conditions at the start can set you up for success later on. This podcast will discuss our labs efforts to setup chromatographic conditions for the analysis of ethyl-glucuronide and buprenorphine (plus metabolites).</itunes:subtitle>
      <itunes:keywords>msacl, mass spectrometry, chromatography, clinical, connect</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>3</itunes:episode>
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      <title>Vitamin D and Immune Function</title>
      <description><![CDATA[<p>Prof. Hewison’s group is at the forefront of research linking vitamin D and the immune system, with implications for a wide range of clinical disorders including infectious, inflammatory and autoimmune disease. Current studies are focused on the analysis of vitamin D-insensitivity in T lymphocytes from the inflamed joints of patients with rheumatoid arthritis. This may provide an explanation for the limited success of vitamin D supplementation in some clinical trials. Other projects have explored the role of cell metabolism pathways in mediating the immunomodulatory effects of vitamin D, and the opportunities this may provide for improved therapeutic use of vitamin D. The Hewison group has also pioneered a range of studies to explore alternative markers of vitamin D ‘status’. This includes development of novel high throughput liquid chromatography-tandem mass spectrometry technology to measure multiple metabolites of vitamin D – the vitamin D metabolome – and analysis of the role of the serum vitamin D binding protein as a determinant of vitamin D bioavailability within the immune system.</p>
]]></description>
      <pubDate>Tue, 8 Dec 2020 18:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (Martin Hewison)</author>
      <link>https://msacl.simplecast.com/episodes/vitamin-d-and-immune-function-RDexEb3W</link>
      <content:encoded><![CDATA[<p>Prof. Hewison’s group is at the forefront of research linking vitamin D and the immune system, with implications for a wide range of clinical disorders including infectious, inflammatory and autoimmune disease. Current studies are focused on the analysis of vitamin D-insensitivity in T lymphocytes from the inflamed joints of patients with rheumatoid arthritis. This may provide an explanation for the limited success of vitamin D supplementation in some clinical trials. Other projects have explored the role of cell metabolism pathways in mediating the immunomodulatory effects of vitamin D, and the opportunities this may provide for improved therapeutic use of vitamin D. The Hewison group has also pioneered a range of studies to explore alternative markers of vitamin D ‘status’. This includes development of novel high throughput liquid chromatography-tandem mass spectrometry technology to measure multiple metabolites of vitamin D – the vitamin D metabolome – and analysis of the role of the serum vitamin D binding protein as a determinant of vitamin D bioavailability within the immune system.</p>
]]></content:encoded>
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      <itunes:title>Vitamin D and Immune Function</itunes:title>
      <itunes:author>Martin Hewison</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/1bd82ac6-2071-4c73-a174-e74f1dca45c1/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>01:29:37</itunes:duration>
      <itunes:summary>An overview  of the impact that Vitamin D status has on the immune system.</itunes:summary>
      <itunes:subtitle>An overview  of the impact that Vitamin D status has on the immune system.</itunes:subtitle>
      <itunes:keywords>vitamin d, immune function, immune system, covid</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>2</itunes:episode>
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      <title>Getting going with MS (1) : Josh installs a mass spectrometer</title>
      <description><![CDATA[<table><tbody><tr><td>This session will serve as an introduction to a 4 part series in which Dr. Hayden will invite attendees to witness in real time his journey bringing mass spec testing to a clinical lab. During these interactive sessions, attendees will be encouraged to help troubleshoot, and offer advice as desired.<br /><br />Subsequent sessions anticipated include:<br />1. Getting going with mass spectrometry: Josh learns chromatography<br />2. Getting going with mass spectrometry: Josh tries to do sample preparation<br />3. Getting going with mass spectrometry: Josh analyzes peaks</td></tr></tbody></table>
]]></description>
      <pubDate>Thu, 22 Oct 2020 17:00:00 +0000</pubDate>
      <author>chris.herold@msacl.org (MSACL)</author>
      <link>https://msacl.simplecast.com/episodes/getting-going-with-mass-spectrometry-josh-installs-a-mass-spectrometer-lw0UPA1p</link>
      <content:encoded><![CDATA[<table><tbody><tr><td>This session will serve as an introduction to a 4 part series in which Dr. Hayden will invite attendees to witness in real time his journey bringing mass spec testing to a clinical lab. During these interactive sessions, attendees will be encouraged to help troubleshoot, and offer advice as desired.<br /><br />Subsequent sessions anticipated include:<br />1. Getting going with mass spectrometry: Josh learns chromatography<br />2. Getting going with mass spectrometry: Josh tries to do sample preparation<br />3. Getting going with mass spectrometry: Josh analyzes peaks</td></tr></tbody></table>
]]></content:encoded>
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      <itunes:title>Getting going with MS (1) : Josh installs a mass spectrometer</itunes:title>
      <itunes:author>MSACL</itunes:author>
      <itunes:image href="https://image.simplecastcdn.com/images/2047208e-076d-4901-bf87-51a4cd6e8d82/2f463e9d-8a61-4236-917e-ef7eb1925083/3000x3000/msacl-connect-3000x3000-v01-for-podcasts.jpg?aid=rss_feed"/>
      <itunes:duration>00:50:05</itunes:duration>
      <itunes:summary>The applications of mass spectrometry in the clinical laboratory continue to expand. Unfortunately, not all clinical laboratories have mass spectrometers and there are substantial barriers to bringing in this instrumentation. This webinar will discuss some of these barriers and how we have been able to overcome them in our path towards setting up clinical mass spectrometry testing.</itunes:summary>
      <itunes:subtitle>The applications of mass spectrometry in the clinical laboratory continue to expand. Unfortunately, not all clinical laboratories have mass spectrometers and there are substantial barriers to bringing in this instrumentation. This webinar will discuss some of these barriers and how we have been able to overcome them in our path towards setting up clinical mass spectrometry testing.</itunes:subtitle>
      <itunes:keywords>msacl, troubleshooting, mass spectrometry, clinical</itunes:keywords>
      <itunes:explicit>no</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>1</itunes:episode>
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