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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
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  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/article/10.1186/s13039-024-00698-w.

Title:
Precision oncology platforms: practical strategies for genomic database utilization in cancer treatment | Molecular Cytogenetics
Description:
In recent years, the expansion of molecularly targeted cancer therapies has significantly advanced precision oncology. Parallel developments in next-generation sequencing (NGS) technologies have also improved precision oncology applications, making genomic analysis of tumors more affordable and accessible. Targeted NGS panels now enable the rapid identification of diverse actionable mutations, requiring clinicians to efficiently assess the predictive value of cancer biomarkers for specific treatments. The urgency for timely and accurate decision-making in oncology emphasizes the importance of reliable precision oncology software. Online clinical decision-making tools and associated cancer databases have been designed by consolidating genomic data into standardized, accessible formats. These new platforms are highly integrated and crucial for identifying actionable somatic genomic biomarkers essential for tumor survival, determining corresponding drug targets, and selecting appropriate treatments based on the mutational profile of each patient’s tumor. To help oncologists and translational cancer researchers unfamiliar with these tools, we review the utility, accuracy, and comprehensiveness of several commonly used precision medicine software options currently available. Our analysis categorized selected genomic databases based on their primary content, utility, and how well they provide practical guidance for interpreting somatic biomarker data. We identified several comprehensive, mostly open-access platforms that are easy to use for genetic biomarker searches, each with unique features and limitations. Among the precision oncology tools we evaluated, we found MyCancerGenome and OncoKB to be the first choice, offering comprehensive, accurate up-to-date information on the clinical significance of somatic mutations. To illustrate the application of these precision oncology tools in clinical settings, we evaluated three case studies to see how use of the platforms could have influenced treatment planning. Most of the precision oncology software evaluated could be easily streamlined into clinical workflows to provide updated information on approved drugs and clinical trials related the actionable mutations detected. Some platforms were very intuitive and easy to use, while others, often developed in smaller academic settings, were more difficult to navigate and may not be updated consistently. Future enhancements, incorporating artificial intelligence algorithms, are likely to improve integration of the platforms with diverse big data sources, enabling more accurate predictions of potential therapeutic responses.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,626,182 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

cancer, clinical, data, platform, information, genomic, platforms, evidence, mutations, pubmed, users, search, gene, drug, article, mutation, tumor, variants, treatment, specific, google, scholar, genes, precision, database, drugs, databases, alterations, response, therapies, trials, including, somatic, studies, updated, research, oncology, types, variant, biomarkers, case, level, list, access, potential, based, researchers, analysis, comprehensive, therapeutic,

Topics {✒️}

/solutions/mmportal-clinical-decision-support multi-omics integration database large-scale genomic cohorts amp/asco/cap somatic guidelines dna copy-number variations circulating tumor dna tumor expressed pd-l1 personalized cancer therapy—leveraging incorporate multi-omics data egfr tyrosine-kinase inhibitors large-scale public repository artificial intelligence support clinical decision-making informed decision-making based pd-l1 expression level ngs-based multiplex assay aid clinical decision-making include egfr tyrosine-kinase dna methylation data memorial sloan kettering thirty-day free trial small-cell lung carcinoma cancer-related biological activities relevant pubmed articles structured clinical-grade mutations personalized cancer treatment suspected deleterious brca-mutation article download pdf braf wild-type status efgr t790m-mutated cases large-scale project personalized cancer therapy platinum-based chemotherapy personalized treatment plans interactive gene/drug heatmap somatic mutational profiles underwent empiric chemotherapy privacy choices/manage cookies drug–gene interaction database potential decreased sensitivity/resistance fda-approved therapies relating leticia frohlich archangelo amp/asco/cap rees mg seashore-ludlow org/research/standards/onc_path_sop/ disease-focused expert groups molecular oncology knowledgebase precision oncology databases natural language processing

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Precision oncology platforms: practical strategies for genomic database utilization in cancer treatment
         description:In recent years, the expansion of molecularly targeted cancer therapies has significantly advanced precision oncology. Parallel developments in next-generation sequencing (NGS) technologies have also improved precision oncology applications, making genomic analysis of tumors more affordable and accessible. Targeted NGS panels now enable the rapid identification of diverse actionable mutations, requiring clinicians to efficiently assess the predictive value of cancer biomarkers for specific treatments. The urgency for timely and accurate decision-making in oncology emphasizes the importance of reliable precision oncology software. Online clinical decision-making tools and associated cancer databases have been designed by consolidating genomic data into standardized, accessible formats. These new platforms are highly integrated and crucial for identifying actionable somatic genomic biomarkers essential for tumor survival, determining corresponding drug targets, and selecting appropriate treatments based on the mutational profile of each patient’s tumor. To help oncologists and translational cancer researchers unfamiliar with these tools, we review the utility, accuracy, and comprehensiveness of several commonly used precision medicine software options currently available. Our analysis categorized selected genomic databases based on their primary content, utility, and how well they provide practical guidance for interpreting somatic biomarker data. We identified several comprehensive, mostly open-access platforms that are easy to use for genetic biomarker searches, each with unique features and limitations. Among the precision oncology tools we evaluated, we found MyCancerGenome and OncoKB to be the first choice, offering comprehensive, accurate up-to-date information on the clinical significance of somatic mutations. To illustrate the application of these precision oncology tools in clinical settings, we evaluated three case studies to see how use of the platforms could have influenced treatment planning. Most of the precision oncology software evaluated could be easily streamlined into clinical workflows to provide updated information on approved drugs and clinical trials related the actionable mutations detected. Some platforms were very intuitive and easy to use, while others, often developed in smaller academic settings, were more difficult to navigate and may not be updated consistently. Future enhancements, incorporating artificial intelligence algorithms, are likely to improve integration of the platforms with diverse big data sources, enabling more accurate predictions of potential therapeutic responses.
         datePublished:2024-11-14T00:00:00Z
         dateModified:2024-11-14T00:00:00Z
         pageStart:1
         pageEnd:18
         license:http://creativecommons.org/licenses/by-nc-nd/4.0/
         sameAs:https://doi.org/10.1186/s13039-024-00698-w
         keywords:
            Oncogenes
            Tumor suppressor genes
            DNA mutational analysis
            Personalized cancer treatment
            Cancer biomarkers
            Chemotherapy
            Actionable mutations
            Artificial intelligence
            Big data integration
            Oncology software
            Cytogenetics
            Molecular Medicine
            Human Genetics
         image:
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         isPartOf:
            name:Molecular Cytogenetics
            issn:
               1755-8166
            volumeNumber:17
            type:
               Periodical
               PublicationVolume
         publisher:
            name:BioMed Central
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:Antonia A. Gazola
               affiliation:
                     name:Pontifical Catholic University of Rio Grande do Sul - PUCRS
                     address:
                        name:School of Medicine, Pontifical Catholic University of Rio Grande do Sul - PUCRS, Porto Alegre, Brazil
                        type:PostalAddress
                     type:Organization
               type:Person
               name:William Lautert-Dutra
               affiliation:
                     name:University of Sao Paulo – USP
                     address:
                        name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Leticia Frohlich Archangelo
               affiliation:
                     name:University of Sao Paulo (FMRP-USP)
                     address:
                        name:Department of Cellular and Molecular Biology and Pathogenic Bioagents, Medical School of Ribeirao Preto, University of Sao Paulo (FMRP-USP), Ribeirao Preto, Brazil
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Rodolfo B. dos Reis
               affiliation:
                     name:University of Sao Paulo – USP
                     address:
                        name:Division of Urology, Department of Surgery and Anatomy, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Jeremy A. Squire
               affiliation:
                     name:University of Sao Paulo – USP
                     address:
                        name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
                        type:PostalAddress
                     type:Organization
                     name:Queen’s University
                     address:
                        name:Department of Pathology and Molecular Medicine, Queen’s University, Kingston, Canada
                        type:PostalAddress
                     type:Organization
               email:[email protected]
               type:Person
         isAccessibleForFree:1
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Precision oncology platforms: practical strategies for genomic database utilization in cancer treatment
      description:In recent years, the expansion of molecularly targeted cancer therapies has significantly advanced precision oncology. Parallel developments in next-generation sequencing (NGS) technologies have also improved precision oncology applications, making genomic analysis of tumors more affordable and accessible. Targeted NGS panels now enable the rapid identification of diverse actionable mutations, requiring clinicians to efficiently assess the predictive value of cancer biomarkers for specific treatments. The urgency for timely and accurate decision-making in oncology emphasizes the importance of reliable precision oncology software. Online clinical decision-making tools and associated cancer databases have been designed by consolidating genomic data into standardized, accessible formats. These new platforms are highly integrated and crucial for identifying actionable somatic genomic biomarkers essential for tumor survival, determining corresponding drug targets, and selecting appropriate treatments based on the mutational profile of each patient’s tumor. To help oncologists and translational cancer researchers unfamiliar with these tools, we review the utility, accuracy, and comprehensiveness of several commonly used precision medicine software options currently available. Our analysis categorized selected genomic databases based on their primary content, utility, and how well they provide practical guidance for interpreting somatic biomarker data. We identified several comprehensive, mostly open-access platforms that are easy to use for genetic biomarker searches, each with unique features and limitations. Among the precision oncology tools we evaluated, we found MyCancerGenome and OncoKB to be the first choice, offering comprehensive, accurate up-to-date information on the clinical significance of somatic mutations. To illustrate the application of these precision oncology tools in clinical settings, we evaluated three case studies to see how use of the platforms could have influenced treatment planning. Most of the precision oncology software evaluated could be easily streamlined into clinical workflows to provide updated information on approved drugs and clinical trials related the actionable mutations detected. Some platforms were very intuitive and easy to use, while others, often developed in smaller academic settings, were more difficult to navigate and may not be updated consistently. Future enhancements, incorporating artificial intelligence algorithms, are likely to improve integration of the platforms with diverse big data sources, enabling more accurate predictions of potential therapeutic responses.
      datePublished:2024-11-14T00:00:00Z
      dateModified:2024-11-14T00:00:00Z
      pageStart:1
      pageEnd:18
      license:http://creativecommons.org/licenses/by-nc-nd/4.0/
      sameAs:https://doi.org/10.1186/s13039-024-00698-w
      keywords:
         Oncogenes
         Tumor suppressor genes
         DNA mutational analysis
         Personalized cancer treatment
         Cancer biomarkers
         Chemotherapy
         Actionable mutations
         Artificial intelligence
         Big data integration
         Oncology software
         Cytogenetics
         Molecular Medicine
         Human Genetics
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13039-024-00698-w/MediaObjects/13039_2024_698_Fig1_HTML.png
      isPartOf:
         name:Molecular Cytogenetics
         issn:
            1755-8166
         volumeNumber:17
         type:
            Periodical
            PublicationVolume
      publisher:
         name:BioMed Central
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Antonia A. Gazola
            affiliation:
                  name:Pontifical Catholic University of Rio Grande do Sul - PUCRS
                  address:
                     name:School of Medicine, Pontifical Catholic University of Rio Grande do Sul - PUCRS, Porto Alegre, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:William Lautert-Dutra
            affiliation:
                  name:University of Sao Paulo – USP
                  address:
                     name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Leticia Frohlich Archangelo
            affiliation:
                  name:University of Sao Paulo (FMRP-USP)
                  address:
                     name:Department of Cellular and Molecular Biology and Pathogenic Bioagents, Medical School of Ribeirao Preto, University of Sao Paulo (FMRP-USP), Ribeirao Preto, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Rodolfo B. dos Reis
            affiliation:
                  name:University of Sao Paulo – USP
                  address:
                     name:Division of Urology, Department of Surgery and Anatomy, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jeremy A. Squire
            affiliation:
                  name:University of Sao Paulo – USP
                  address:
                     name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
                     type:PostalAddress
                  type:Organization
                  name:Queen’s University
                  address:
                     name:Department of Pathology and Molecular Medicine, Queen’s University, Kingston, Canada
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      isAccessibleForFree:1
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      name:Molecular Cytogenetics
      issn:
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      volumeNumber:17
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      name:BioMed Central
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         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
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      name:Pontifical Catholic University of Rio Grande do Sul - PUCRS
      address:
         name:School of Medicine, Pontifical Catholic University of Rio Grande do Sul - PUCRS, Porto Alegre, Brazil
         type:PostalAddress
      name:University of Sao Paulo – USP
      address:
         name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
         type:PostalAddress
      name:University of Sao Paulo (FMRP-USP)
      address:
         name:Department of Cellular and Molecular Biology and Pathogenic Bioagents, Medical School of Ribeirao Preto, University of Sao Paulo (FMRP-USP), Ribeirao Preto, Brazil
         type:PostalAddress
      name:University of Sao Paulo – USP
      address:
         name:Division of Urology, Department of Surgery and Anatomy, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
         type:PostalAddress
      name:University of Sao Paulo – USP
      address:
         name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
         type:PostalAddress
      name:Queen’s University
      address:
         name:Department of Pathology and Molecular Medicine, Queen’s University, Kingston, Canada
         type:PostalAddress
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      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Antonia A. Gazola
      affiliation:
            name:Pontifical Catholic University of Rio Grande do Sul - PUCRS
            address:
               name:School of Medicine, Pontifical Catholic University of Rio Grande do Sul - PUCRS, Porto Alegre, Brazil
               type:PostalAddress
            type:Organization
      name:William Lautert-Dutra
      affiliation:
            name:University of Sao Paulo – USP
            address:
               name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
               type:PostalAddress
            type:Organization
      name:Leticia Frohlich Archangelo
      affiliation:
            name:University of Sao Paulo (FMRP-USP)
            address:
               name:Department of Cellular and Molecular Biology and Pathogenic Bioagents, Medical School of Ribeirao Preto, University of Sao Paulo (FMRP-USP), Ribeirao Preto, Brazil
               type:PostalAddress
            type:Organization
      name:Rodolfo B. dos Reis
      affiliation:
            name:University of Sao Paulo – USP
            address:
               name:Division of Urology, Department of Surgery and Anatomy, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
               type:PostalAddress
            type:Organization
      name:Jeremy A. Squire
      affiliation:
            name:University of Sao Paulo – USP
            address:
               name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
               type:PostalAddress
            type:Organization
            name:Queen’s University
            address:
               name:Department of Pathology and Molecular Medicine, Queen’s University, Kingston, Canada
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:School of Medicine, Pontifical Catholic University of Rio Grande do Sul - PUCRS, Porto Alegre, Brazil
      name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
      name:Department of Cellular and Molecular Biology and Pathogenic Bioagents, Medical School of Ribeirao Preto, University of Sao Paulo (FMRP-USP), Ribeirao Preto, Brazil
      name:Division of Urology, Department of Surgery and Anatomy, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
      name:Department of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo – USP, Ribeirao Preto, Brazil
      name:Department of Pathology and Molecular Medicine, Queen’s University, Kingston, Canada

External Links {🔗}(208)

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