decipher.sanger.ac.uk Report : Visit Site


  • Ranking Alexa Global: # 100,713

    The main IP address: 193.62.203.164,Your server United Kingdom,Cambridge ISP:European Bioinformatics Institute  TLD:uk CountryCode:GB

    The description :decipher helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide...

    This report updates in 10-Jun-2018

Technical data of the decipher.sanger.ac.uk


Geo IP provides you such as latitude, longitude and ISP (Internet Service Provider) etc. informations. Our GeoIP service found where is host decipher.sanger.ac.uk. Currently, hosted in United Kingdom and its service provider is European Bioinformatics Institute .

Latitude: 51.733329772949
Longitude: -2.3666698932648
Country: United Kingdom (GB)
City: Cambridge
Region: England
ISP: European Bioinformatics Institute

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HTTP Header Analysis


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IP:193.62.203.163
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HtmlToText

your browser is out of date . it has known security and performance flaws, and may not display all features of this and other websites. we highly recommend using google chrome or firefox for the best experience with our website. learn how to update your browser. we no longer support logging in with your browser version. about browse genome browser phenotype browser genes syndromes gene disorders ddd(uk) active filters you should only search for one band, gene, or position at a time. e.g. brca2 , short stature , missense_variant , more... clear filters close clear filters search mapping the clinical genome explore decipher it’s free and you don’t need to log in decipher is used by the clinical community to share and compare phenotypic and genotypic data. the decipher database contains data from 26232 patients who have given consent for broad data-sharing; decipher also supports more limited sharing via consortia. have a look at the numbers . anyone can browse publicly-available patient data on decipher and request to be put in contact with the responsible clinician. why? because sharing benefits everyone. explore decipher’s genome browser delve into the human phenotype ontology search all open-access decipher data join decipher be part of the sharing community projects affiliated to decipher can deposit and share patients, variants, and phenotypes to invite collaboration and facilitate diagnosis. once deposited, you can use decipher to identify and prioritise potential matches, and you can request notifications as soon as new matches arrive. as well as influencing individual patient outcomes, use of decipher has contributed to over 1000 published articles since 2004 . it's still free, and you are in control of what data to make public. join now find out more already a member? log in to access your patient data email address password login and password changing are disabled in your browser log in reset your password latest news essential system upgrades wednesday 6 june there will be significant disruption to this service on wednesday 6 june due toessential system upgrades. it is likely that disruption will extend beyond our usual weekly at-risk period, and the service should be considered at risk for the whole day. we apologise for any inconvenience this may cause. update: this work is now complete. decipher 9.23 released we released version 9.23 of decipher on the 23rd of may, 2018. improvements include: the incorporation of the january 2018 clingen sequence variant interpretation working group ( clingen svi ) bayesian classification framework to assist users interpreting acmg pathogenicity evidence. this framework provides a mathematical foundation for what was a qualitative heuristic. the addition of guidance, when users are recording pathogenicity evidence, from clingen svi on the use of acmg criteria pp5 and bp6 (reputable source criteria). these criteria reply on assertions in the absence of primary evidence. decipher v9.22 released we released version 9.22 of decipher on the 25th of april, 2018. improvements include: homozygous and hemizygous gnomad variants are now displayed on the protein browser. the new tracks allow the visualisation of protein changing and loss of function homozygous and hemizygous gnomad variants. images of relevant amino acids are now displayed for missense sequence variants on the consequence prediction (vep) tab in patient records. input values for cardiac conditions for calculating the maximum tolerated population allele frequency are now displayed in decipher. the tolerated population variation calculator can be used to determine whether a variant observed in the reference sample is too common to cause a given mendelian disorder of interest. the decipher pathogencitiy class definitely pathogenic” has been changed to “pathogenic” in line with acmg and acgs nomenclature. for more news about decipher, click here . citing decipher decipher: database of chromosomal imbalance and phenotype in humans using ensembl resources. firth, h.v. et al (2009). am.j.hum.genet 84, 524-533 (doi: dx.doi.org/10/1016/j.ajhg.2009.03.010 ) authors who use data from the project must acknowledge decipher using the following wording: "this study makes use of data generated by the decipher community. a full list of centres who contributed to the generation of the data is available from http://decipher.sanger.ac.uk and via email from [email protected]. funding for the project was provided by wellcome." please see citing decipher for more information. feedback information about decipher advisory board affiliations project proposal downloads ethical framework data flowchart data files forms consent assent family pack policies cookies policy disclaimer legal data sharing report a bug | feedback [email protected] wellcome sanger institute genome research limited (reg no. 2742969) is a charity registered in england with number 1021457

URL analysis for decipher.sanger.ac.uk


https://decipher.sanger.ac.uk/

Whois Information


Whois is a protocol that is access to registering information. You can reach when the website was registered, when it will be expire, what is contact details of the site with the following informations. In a nutshell, it includes these informations;


No such domain ac.uk


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SERVERS

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