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Title | Clinical Sequencing Evidence-Generating Research | |
Description | Log in News Projects Publications Resources Research Materials Clinical Sequencing Evidence-Generating Research The Clinical Sequencing Evidence-Generatin |
Keywords | N/A |
WebSite | cser-consortium.org |
Host IP | 128.95.55.209 |
Location | United States |
Site | Rank |
US$2,315,368
Last updated: 2023-05-14 02:38:12
cser-consortium.org has Semrush global rank of 4,571,328. cser-consortium.org has an estimated worth of US$ 2,315,368, based on its estimated Ads revenue. cser-consortium.org receives approximately 267,158 unique visitors each day. Its web server is located in United States, with IP address 128.95.55.209. According to SiteAdvisor, cser-consortium.org is safe to visit. |
Purchase/Sale Value | US$2,315,368 |
Daily Ads Revenue | US$2,138 |
Monthly Ads Revenue | US$64,118 |
Yearly Ads Revenue | US$769,415 |
Daily Unique Visitors | 17,811 |
Note: All traffic and earnings values are estimates. |
Host | Type | TTL | Data |
cser-consortium.org. | A | 86400 | IP: 128.95.55.209 |
cser-consortium.org. | NS | 86400 | NS Record: marge.cac.washington.edu. |
cser-consortium.org. | NS | 86400 | NS Record: holly.s.uw.edu. |
cser-consortium.org. | NS | 86400 | NS Record: hanna.cac.washington.edu. |
Log in News Projects Publications Resources Research Materials Clinical Sequencing Evidence-Generating Research The Clinical Sequencing Evidence-Generating Research (CSER) consortium is a national multi-site research program funded by the National Human Genome Research Institute (NHGRI), the National Cancer Institute (NCI) and the National Institute on Minority Health and Health Disparities (NIMHD). Prioritizing engagement of traditionally underrepresented populations in genomics research, CSER’s seven clinical sites seek to study the effectiveness of integrating genome sequencing into the clinical care of diverse and medically underserved individuals. CSER’s research goals include measuring sequencing’s clinical utility through patient and familial responses to genomic testing and evaluating patient-provider-laboratory interactions that influence the use of sequencing. Drawing from the expertise of clinicians, scientists, ethicists, bioinformaticians, economists, and legal scholars, |
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