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  1. Article ; Online: VarGrouper: A Bioinformatic Tool for Local Haplotyping of Deletion-Insertion Variants from Next-Generation Sequencing Data after Variant Calling.

    Schmidt, Ryan J / Macleay, Allison / Le, Long Phi

    The Journal of molecular diagnostics : JMD

    2019  Volume 21, Issue 3, Page(s) 384–389

    Abstract: Accurate genetic variant representation through nomenclature and annotation is essential for understanding functional consequence and properly noting the presence of variants across time, assays, and laboratories. Current variant calling algorithms ... ...

    Abstract Accurate genetic variant representation through nomenclature and annotation is essential for understanding functional consequence and properly noting the presence of variants across time, assays, and laboratories. Current variant calling algorithms detect single deletion-insertion variants as multiple indel and/or substitution variants from next-generation sequencing data. Consequently, these variants are separately annotated in bioinformatics pipelines, leading to inaccurate variant representation. We developed a bioinformatic solution to this problem-VarGrouper-that automatically recognizes individual variants that arise from a deletion-insertion variant and aggregates them into a single variant that can be properly annotated. This tool has been integrated into our routine clinical molecular diagnostics workflow for DNA sequencing of solid tumors. Over an 11-month period, VarGrouper variants were reported by all attending molecular pathologists involved in interpretation and represented 4.1% of all variants reported; 10.9% of cases with reportable variants contained at least one VarGrouper variant. VarGrouper improves the practice of molecular diagnostics by increasing the accuracy and consistency of variant annotation. VarGrouper is freely available for use by the molecular diagnostic community.
    MeSH term(s) Algorithms ; Base Sequence ; Computational Biology/methods ; Haplotypes/genetics ; High-Throughput Nucleotide Sequencing/methods ; Humans ; INDEL Mutation/genetics ; Software
    Language English
    Publishing date 2019-02-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2000060-1
    ISSN 1943-7811 ; 1525-1578
    ISSN (online) 1943-7811
    ISSN 1525-1578
    DOI 10.1016/j.jmoldx.2018.12.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Design and implementation of an automated email notification system for results of tests pending at discharge.

    Dalal, Anuj K / Schnipper, Jeffrey L / Poon, Eric G / Williams, Deborah H / Rossi-Roh, Kathleen / Macleay, Allison / Liang, Catherine L / Nolido, Nyryan / Budris, Jonas / Bates, David W / Roy, Christopher L

    Journal of the American Medical Informatics Association : JAMIA

    2012  Volume 19, Issue 4, Page(s) 523–528

    Abstract: Physicians are often unaware of the results of tests pending at discharge (TPADs). The authors designed and implemented an automated system to notify the responsible inpatient physician of the finalized results of TPADs using secure, network email. The ... ...

    Abstract Physicians are often unaware of the results of tests pending at discharge (TPADs). The authors designed and implemented an automated system to notify the responsible inpatient physician of the finalized results of TPADs using secure, network email. The system coordinates a series of electronic events triggered by the discharge time stamp and sends an email to the identified discharging attending physician once finalized results are available. A carbon copy is sent to the primary care physicians in order to facilitate communication and the subsequent transfer of responsibility. Logic was incorporated to suppress selected tests and to limit notification volume. The system was activated for patients with TPADs discharged by randomly selected inpatient-attending physicians during a 6-month pilot. They received approximately 1.6 email notifications per discharged patient with TPADs. Eighty-four per cent of inpatient-attending physicians receiving automated email notifications stated that they were satisfied with the system in a brief survey (59% survey response rate). Automated email notification is a useful strategy for managing results of TPADs.
    MeSH term(s) Automation ; Boston ; Consumer Behavior ; Diagnostic Techniques and Procedures ; Electronic Mail ; Humans ; Patient Discharge ; Pilot Projects
    Language English
    Publishing date 2012-01-19
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 1205156-1
    ISSN 1527-974X ; 1067-5027
    ISSN (online) 1527-974X
    ISSN 1067-5027
    DOI 10.1136/amiajnl-2011-000615
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Expressed Gene Fusions as Frequent Drivers of Poor Outcomes in Hormone Receptor-Positive Breast Cancer.

    Matissek, Karina J / Onozato, Maristela L / Sun, Sheng / Zheng, Zongli / Schultz, Andrew / Lee, Jesse / Patel, Kristofer / Jerevall, Piiha-Lotta / Saladi, Srinivas Vinod / Macleay, Allison / Tavallai, Mehrad / Badovinac-Crnjevic, Tanja / Barrios, Carlos / Beşe, Nuran / Chan, Arlene / Chavarri-Guerra, Yanin / Debiasi, Marcio / Demirdögen, Elif / Egeli, Ünal /
    Gökgöz, Sahsuvar / Gomez, Henry / Liedke, Pedro / Tasdelen, Ismet / Tolunay, Sahsine / Werutsky, Gustavo / St Louis, Jessica / Horick, Nora / Finkelstein, Dianne M / Le, Long Phi / Bardia, Aditya / Goss, Paul E / Sgroi, Dennis C / Iafrate, A John / Ellisen, Leif W

    Cancer discovery

    2017  Volume 8, Issue 3, Page(s) 336–353

    Abstract: We sought to uncover genetic drivers of hormone receptor-positive ( ... ...

    Abstract We sought to uncover genetic drivers of hormone receptor-positive (HR
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Animals ; Breast Neoplasms/drug therapy ; Breast Neoplasms/genetics ; Breast Neoplasms/mortality ; Breast Neoplasms/pathology ; Cell Line, Tumor ; Class I Phosphatidylinositol 3-Kinases/genetics ; Estrogen Receptor alpha/genetics ; Female ; Gene Expression Regulation, Neoplastic ; Gene Fusion ; Heterocyclic Compounds, 3-Ring/pharmacology ; Humans ; Mice, Nude ; Middle Aged ; Protein Kinase Inhibitors/pharmacology ; Proto-Oncogene Proteins c-akt/genetics ; Proto-Oncogene Proteins c-akt/metabolism ; Proto-Oncogene Proteins c-raf/genetics ; Pyridones/pharmacology ; Pyrimidinones/pharmacology ; Receptors, Steroid/metabolism ; Ribosomal Protein S6 Kinases/genetics ; Ribosomal Protein S6 Kinases/metabolism ; Xenograft Model Antitumor Assays
    Chemical Substances ESR1 protein, human ; Estrogen Receptor alpha ; Heterocyclic Compounds, 3-Ring ; MK 2206 ; Protein Kinase Inhibitors ; Pyridones ; Pyrimidinones ; Receptors, Steroid ; trametinib (33E86K87QN) ; Class I Phosphatidylinositol 3-Kinases (EC 2.7.1.137) ; PIK3CA protein, human (EC 2.7.1.137) ; AKT3 protein, human (EC 2.7.11.1) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1) ; Proto-Oncogene Proteins c-raf (EC 2.7.11.1) ; RPS6KC1 protein, human (EC 2.7.11.1) ; Raf1 protein, human (EC 2.7.11.1) ; Ribosomal Protein S6 Kinases (EC 2.7.11.1)
    Language English
    Publishing date 2017-12-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2625242-9
    ISSN 2159-8290 ; 2159-8274
    ISSN (online) 2159-8290
    ISSN 2159-8274
    DOI 10.1158/2159-8290.CD-17-0535
    Database MEDical Literature Analysis and Retrieval System OnLINE

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