kidsgenomics.org valuation and analysis

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Sitemap: http://kidsgenomics.org/news-sitemap.xml
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Title KidsGenomics - Next-generation genomics for rare diseases and
Description Next-generation genomics for rare diseases and pediatric
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WebSite kidsgenomics faviconkidsgenomics.org
Host IP 160.153.49.162
Location United States
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kidsgenomics.org Valuation
US$821,480
Last updated: 2022-06-12 08:54:34

kidsgenomics.org has Semrush global rank of 12,884,434. kidsgenomics.org has an estimated worth of US$ 821,480, based on its estimated Ads revenue. kidsgenomics.org receives approximately 94,787 unique visitors each day. Its web server is located in United States, with IP address 160.153.49.162. According to SiteAdvisor, kidsgenomics.org is safe to visit.

Traffic & Worth Estimates
Purchase/Sale Value US$821,480
Daily Ads Revenue US$759
Monthly Ads Revenue US$22,749
Yearly Ads Revenue US$272,985
Daily Unique Visitors 6,320
Note: All traffic and earnings values are estimates.
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Host Type TTL Data
kidsgenomics.org. A 10800 IP: 160.153.49.162
kidsgenomics.org. NS 3600 NS Record: ns11.domaincontrol.com.
kidsgenomics.org. NS 3600 NS Record: ns12.domaincontrol.com.
kidsgenomics.org. MX 3600 MX Record: 0 kidsgenomics-org.mail.protection.outlook.com.
kidsgenomics.org. TXT 3600 TXT Record: NETORGFT8755382.onmicrosoft.com
kidsgenomics.org. TXT 3600 TXT Record: v=spf1 include:secureserver.net -all
HtmlToTextCheckTime:2022-06-12 08:54:34
Skip to content Skip to primary sidebar Main navigation About Research Contact Subscribe Support KidsGenomics Next-generation genomics for rare diseases and pediatric cancers Origins and Cautions for the gnomAD Database March 1, 2022 by dkoboldt Leave a Comment High-throughput sequencing has accelerated human genetics research in countless ways, from rapid newborn sequencing to Mendelian disorders to the many discoveries being made in common, complex disease cohorts. Yet one of the most fundamental benefits of this technology is our ability to catalogue human genetic variation in large cohorts of individuals. For a long while, such catalogues necessarily focused on variation in human protein-coding genes. Coding regions harbor the vast majority of medically-relevant sequence variants — in part because their biological effects are easier to predict — but they only occupy a small 1-2% of the human genome. Whole-genome sequencing offers a far more comprehensive interrogation of genetic
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