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1.
Cancer Cell ; 42(5): 723-726, 2024 May 13.
Artículo en Inglés | MEDLINE | ID: mdl-38701793

RESUMEN

Advances in biomedical research require a robust physician scientist workforce. Despite being equally successful at securing early career awards from the NIH as men, women MD-PhD physician scientists are less likely to serve as principal investigators on mid- and later careers awards. Here, we discuss the causes of gender disparities in academic medicine, the implications of losing highly trained women physician scientists, and the institutional and systemic changes needed to sustain this pool of talented investigators.


Asunto(s)
Investigación Biomédica , Médicos Mujeres , Investigadores , Humanos , Femenino , Médicos Mujeres/estadística & datos numéricos , Masculino , Selección de Profesión , Estados Unidos , Sexismo , Movilidad Laboral , Médicos , Distinciones y Premios
2.
Cancer Inform ; 16: 1176935117711940, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28690394

RESUMEN

ClinicalTrials.org is a popular portal which physicians use to find clinical trials for their patients. However, the current setup of ClinicalTrials.org makes it difficult for oncologists to locate clinical trials for patients based on mutational status. We present CTMine, a system that mines ClinicalTrials.org for clinical trials per cancer mutation and displays the trials in a user-friendly Web application. The system currently lists clinical trials for 6 common genes (ALK, BRAF, ERBB2, EGFR, KIT, and KRAS). The current machine learning model used to identify relevant clinical trials focusing on the above gene mutations had an average 88% precision/recall. As part of this analysis, we compared human versus machine and found that oncologists were unable to reach a consensus on whether a clinical trial mined by CTMine was "relevant" per gene mutation, a finding that highlights an important topic which deems future exploration.

3.
PLoS One ; 12(4): e0175860, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28437440

RESUMEN

Scientists have unprecedented access to a wide variety of high-quality datasets. These datasets, which are often independently curated, commonly use unstructured spreadsheets to store their data. Standardized annotations are essential to perform synthesis studies across investigators, but are often not used in practice. Therefore, accurately combining records in spreadsheets from differing studies requires tedious and error-prone human curation. These efforts result in a significant time and cost barrier to synthesis research. We propose an information retrieval inspired algorithm, Synthesize, that merges unstructured data automatically based on both column labels and values. Application of the Synthesize algorithm to cancer and ecological datasets had high accuracy (on the order of 85-100%). We further implement Synthesize in an open source web application, Synthesizer (https://github.com/lisagandy/synthesizer). The software accepts input as spreadsheets in comma separated value (CSV) format, visualizes the merged data, and outputs the results as a new spreadsheet. Synthesizer includes an easy to use graphical user interface, which enables the user to finish combining data and obtain perfect accuracy. Future work will allow detection of units to automatically merge continuous data and application of the algorithm to other data formats, including databases.


Asunto(s)
Sistemas de Administración de Bases de Datos , Almacenamiento y Recuperación de la Información/métodos , Programas Informáticos , Algoritmos , Bases de Datos Factuales
4.
J Med Internet Res ; 17(6): e154, 2015 Jun 19.
Artículo en Inglés | MEDLINE | ID: mdl-26091775

RESUMEN

BACKGROUND: User content posted through Twitter has been used for biosurveillance, to characterize public perception of health-related topics, and as a means of distributing information to the general public. Most of the existing work surrounding Twitter and health care has shown Twitter to be an effective medium for these problems but more could be done to provide finer and more efficient access to all pertinent data. Given the diversity of user-generated content, small samples or summary presentations of the data arguably omit a large part of the virtual discussion taking place in the Twittersphere. Still, managing, processing, and querying large amounts of Twitter data is not a trivial task. This work describes tools and techniques capable of handling larger sets of Twitter data and demonstrates their use with the issue of antibiotics. OBJECTIVE: This work has two principle objectives: (1) to provide an open-source means to efficiently explore all collected tweets and query health-related topics on Twitter, specifically, questions such as what users are saying and how messages are spread, and (2) to characterize the larger discourse taking place on Twitter with respect to antibiotics. METHODS: Open-source software suites Hadoop, Flume, and Hive were used to collect and query a large number of Twitter posts. To classify tweets by topic, a deep network classifier was trained using a limited number of manually classified tweets. The particular machine learning approach used also allowed the use of a large number of unclassified tweets to increase performance. RESULTS: Query-based analysis of the collected tweets revealed that a large number of users contributed to the online discussion and that a frequent topic mentioned was resistance. A number of prominent events related to antibiotics led to a number of spikes in activity but these were short in duration. The category-based classifier developed was able to correctly classify 70% of manually labeled tweets (using a 10-fold cross validation procedure and 9 classes). The classifier also performed well when evaluated on a per category basis. CONCLUSIONS: Using existing tools such as Hive, Flume, Hadoop, and machine learning techniques, it is possible to construct tools and workflows to collect and query large amounts of Twitter data to characterize the larger discussion taking place on Twitter with respect to a particular health-related topic. Furthermore, using newer machine learning techniques and a limited number of manually labeled tweets, an entire body of collected tweets can be classified to indicate what topics are driving the virtual, online discussion. The resulting classifier can also be used to efficiently explore collected tweets by category and search for messages of interest or exemplary content.


Asunto(s)
Antibacterianos , Farmacorresistencia Microbiana , Internet , Opinión Pública , Medios de Comunicación Sociales , Actitud Frente a la Salud , Humanos , Difusión de la Información , Aprendizaje Automático , Programas Informáticos
5.
Am J Clin Pathol ; 136(6): 848-54, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22095369

RESUMEN

Telavancin (Vibativ, Astellas Pharma US, Deerfield, IL) is a lipoglycopeptide antibiotic that has activity against gram-positive microorganisms, but also has the ability to bind to artificial phospholipids found in coagulation reagents. Normal pooled plasma was spiked with telavancin to obtain concentrations of 0, 12.5, 25, 50, 75, 100, 125, and 150 µg/mL of drug. Samples were tested using 3 different prothrombin time/international normalized ratio (INR) and activated partial thromboplastin time (aPTT) reagent systems, as well as for fibrinogen level, thrombin time, D-dimer level, dilute Russell viper venom time (DRVVT), protein C activity, and protein S activity. There was no effect of telavancin seen with non-phospholipid-dependent assays: fibrinogen level, thrombin time, and D-dimer testing. All INR and aPTT systems demonstrated concentration-dependent increases in clotting times, with Innovin (Siemens Healthcare Diagnostics, Deerfield, IL) INRs the most dramatic. False-positive DRVVT ratios started at 12.5 µg/mL of telavancin, with no effect on protein C or protein S levels until the telavancin level reached more than 100 µg/mL.


Asunto(s)
Aminoglicósidos/farmacología , Coagulación Sanguínea/efectos de los fármacos , Aminoglicósidos/efectos adversos , Pruebas de Coagulación Sanguínea , Esquema de Medicación , Productos de Degradación de Fibrina-Fibrinógeno/efectos de los fármacos , Fibrinógeno/metabolismo , Humanos , Relación Normalizada Internacional , Lipoglucopéptidos , Tiempo de Tromboplastina Parcial , Tiempo de Protrombina , Proteínas Recombinantes/efectos de los fármacos , Proteínas Recombinantes/uso terapéutico , Tiempo de Trombina , Tromboplastina/efectos de los fármacos , Tromboplastina/uso terapéutico
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