1. Center for Medical Genetics and Genomics - UPMC
Our diverse team of medical geneticists and genetic counselors helps families understand genetic disease, provides information about risk factors, and explains ...
Learn more about the Center for Medical Genetics and Genomics at Magee-Womens Hospital of UPMC.
2. Contact | Center for Medical Genetics & Genomics - UPMC
Prenatal/Adult Genetics. UPMC Magee-Womens Hospital 300 Halket St., Suite 1651. Pittsburgh, PA 15213. Phone: 412-641-4168 or 800-454-8155. Fax: 412-641-1032.
Find contact information for the Center for Medical Genetics and Genomics at Magee-Womens Hospital of UPMC.
3. Genetics Locations | UPMC Children's Hospital of Pittsburgh
Within the Genetics Division. Reach that staff within the Division of Genetic and Genomic Medicine at 412-692-5070. Choose option #1 for our scheduling team.
Find a location with Genetics at UPMC Children's Hospital of Pittsburgh.
4. Genetic and Genomic Medicine | Children's Hospital of Pittsburgh
Locations · Providers & Staff · Clinical Services · Genetic Counseling
Genetic and Genomic Medicine at UPMC Children’s Hospital of Pittsburgh is committed to the treatment and study of genetic disorders in children.
5. UPMC Genome Center Team
Here at the UPMC Genome Center, we've assembled a team of experts in clinical and experimental genomics research. Click on “Read more” beneath each team member ...
6. UPMC Precision Medicine Clinic
Our approach integrates traditional primary care/family medicine with a patient's individual characteristics, including genetics, physiology, environmental ...
GENETICS AND PRIMARY CARE PRECISION MEDICINE
7. Genetic and Genomic Medicine - Pitt Pediatrics - University of Pittsburgh
The division's physicians provide genetic services for the Hereditary Telangiectasia Center of Excellence at UPMC and are active in the newly constituted Center ...
The Division of Genetic and Genomic Medicine provides state-of-the-art medical genetics services, as well as generate new information and rapidly incorporate that information into care for children and adults impacted by genetic conditions. The Division consists of five tenure-track faculty members who play highly visible roles in national and international academic societies and government advisory panels. They lead disease-oriented research programs and participate in graduate-level education within the University of Pittsburgh School of Medicine and Graduate School of Public Health.
8. What to expect when you see a genetic counselor
Curious about genetic counseling, and what genetic counselors do? Coach Mandy shares her experience at the UPMC Center for Medical Genetics.
9. UPMC Genome Center Expert High Throughput Next Generation ...
We are a clinical grade, full-service, high-throughput genome center with sequencing options designed for both clinical and research needs. Our dual CAP ...
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10. Dr. Gene & Elizabeth Triano Family Genetics Counseling Fund
The Dr. Gene and Elizabeth Triano Family Genetics Counseling Fund aims to assist with costs for genetic counseling, testing, education, & other preventative and ...
A nonprofit that coordinates charitable giving to support community and educational programs, and resources that improve access to care through UPMC Central Pa.
11. Comparing machine learning screening approaches using ...
12 uur geleden · Please make requests to rashidihh@upmc.edu. Abbreviations. NN: Neural ... genes. BMC Genom. 17(1), 807 (2016). Article Google Scholar. Li ...
Accurate screening of COVID-19 infection status for symptomatic patients is a critical public health task. Although molecular and antigen tests now exist for COVID-19, in resource-limited settings, screening tests are often not available. Furthermore, during the early stages of the pandemic tests were not available in any capacity. We utilized an automated machine learning (ML) approach to train and evaluate thousands of models on a clinical dataset consisting of commonly available clinical and laboratory data, along with cytokine profiles for patients (n = 150). These models were then further tested for generalizability on an out-of-sample secondary dataset (n = 120). We were able to develop a ML model for rapid and reliable screening of patients as COVID-19 positive or negative using three approaches: commonly available clinical and laboratory data, a cytokine profile, and a combination of the common data and cytokine profile. Of the tens of thousands of models automatically tested for the three approaches, all three approaches demonstrated > 92% sensitivity and > 88 specificity while our highest performing model achieved 95.6% sensitivity and 98.1% specificity. These models represent a potential effective deployable solution for COVID-19 status classification for symptomatic patients in resource-limited settings and provide proof-of-concept for rapid development of screening tools for novel emerging infectious diseases.
12. State Board of Medicine - Commonwealth of Pennsylvania
The Board regulates medical doctors; physician assistants; radiology technicians; respiratory therapists; nurse-midwives; acupuncturists; practitioners of ...
The State Board of Medicine regulates the practice of medicine through the licensure, registration and certification of members of the medical profession in the Commonwealth of Pennsylvania.
13. Seattle Children's
One of the best children's hospitals in the country, as ranked by U.S. News & World Report, Seattle Children's Hospital, Foundation and Research Institute ...
One of the best children's hospitals in the country, as ranked by U.S. News & World Report, Seattle Children's Hospital, Foundation and Research Institute advance pediatric care.
14. Utility Analyses of AVITI Sequencing Chemistry - bioRxiv
18 uur geleden · For correspondence: luoj@upmc.edu. 00000000 Comments0 TRiP Peer ... Genetics (12539). Genomics (17202). Immunology (12298). Microbiology ...
Background: DNA sequencing is a critical tool in modern biology. Over the last two decades, it has been revolutionized by the advent of massively parallel sequencing, leading to significant advances in the genome and transcriptome sequencing of various organisms. Nevertheless, challenges with accuracy, lack of competitive options and prohibitive costs associated with high throughput parallel short-read sequencing persist. Results: Here, we conduct a comparative analysis using matched DNA and RNA short-reads assays between Element Biosciences AVITI and Illumina NextSeq 550 chemistries. Similar comparisons were evaluated for synthetic long-read sequencing for RNA and targeted single-cell transcripts between the AVITI and Illumina NovaSeq 6000. For both DNA and RNA short-read applications, the study found that the AVITI produced significantly higher per sequence quality scores. For PCR-free DNA libraries, we observed an average 89.7% lower experimentally determined error rate when using the AVITI chemistry, compared to the NextSeq 550. For short-read RNA quantification, AVITI platform had an average of 32.5% lower error rate than that for NextSeq 550. With regards to synthetic long-read mRNA and targeted synthetic long read single cell mRNA sequencing, both platforms respective chemistries performed comparably in quantification of genes and isoforms. The AVITI displayed a marginally lower error rate for long reads, with fewer chemistry-specific errors and a higher mutation detec...
15. WellSpan Health: Home
Better Healthcare is in Your Genes ... Find out what you can learn from your DNA through WellSpan's community health research program. Sign up for no-cost genetic ...
WellSpan Health is a nationally recognized health system serving South Central Pennsylvania and northern Maryland.
