B-ok.as - TOPMed Imputation Server

nih.gov

https://imputation.biodatacatalyst.nhlbi.nih.gov/

All results are encrypted with a one-time password. After 7 days, all results are deleted from our server. The TOPMed Imputation Server is powered by software invented and developed by the University of Michigan and driven by data provided by the investigators of the TOPMed Program .

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nih.gov

https://topmed.nhlbi.nih.gov/topmed-data-access-scientific-community

Precision Medicine Activities | NHLBI, NIH

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nih.gov

https://www.nhlbi.nih.gov/science/trans-omics-precision-medicine-topmed-program

The TOPMed program has started studies to collect -omics data in a subset of WGS project participants. Currently, these -omics studies are collecting RNA, gene, and metabolite profiles from individuals who participated in the NHLBI-funded Multi-Ethnic Study of Atherosclerosis (MESA).. To help build -omics data, the NHLBI plans to review applications from researchers interested in contributing ...

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nih.gov

https://topmed.nhlbi.nih.gov/awards/2430

Sep 01, 2017 . Introduction slides from 9/1/17 Analysis Committee call This application will bring unprecedented forms of analysis to TOPMed’s already-rich data resources. The application uses recently-developed tools from numerical analysis, that quickly extract key features of the large data summaries used in high-throughput genetic studies. By using them, analyses can be performed on many

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momentum.co.za

https://mmsa.momentum.co.za/mmsa/secure/providers/providersLogin.jsp?fundName=topmed

/Topmed_2007/templateImgs/topMed.jpg" border="0"> Providers Login. Web User Name: Password: Click here for login assistance Click here to request a new password SUBMIT

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readme.io

https://sb-biodatacatalyst.readme.io/docs/topmed-annotation-explorer

The TOPMed Annotation Explorer enables you to interactively explore, query, and study characteristics of an inventory of annotations for the variants called in TOPMed studies. This application can be used pre-association testing, to interactively explore aggregation and filtering strategies for vari...

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topmed.ro

https://www.topmed.ro/

Centrul Medical Topmed Targu-Mures va anunta ca efectueaza un test prenatal premium non-invaziv, denumit NIFTY PRO, care depisteaza Sindromul Down (trisomia 21), alte 5 trisomii precum si alte 87 afectiuni genetice cauzate de suplimentarea sau lipsa de informative genetica in AND-ul fatului.

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imvula.net

https://www.imvula.net/topmed

Topmed Healthcare Distributors is a licensed pharmaceutical wholesaler and distributor operating from a 4000m2 warehouse facility located in Silverton, Pretoria, distributing pharmaceuticals to some 1000 customers nationally, 80% of which are independent pharmacies, whilst the remaining 20% comprises of dispensing doctors, private hospitals, homeopaths and mines.

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medicalaidsearch.co.za

https://www.medicalaidsearch.co.za/topmed

Topmed offers 8 options ranging from R348 to R6 672 p.m. per principal member. Topmed is a registered medical scheme that is passionate about providing a variety of healthcare options that have been specifically formulated to cater to the needs of individuals, SME’s and corporate clients alike.

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nature.com

https://www.nature.com/articles/s41586-021-03205-y

Feb 10, 2021 . Of the 463,182 exome-sequencing variants with MAF > 0.05% in 49,819 participants of the UK Biobank, the majority (84.86%) were also present in …

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webmed.co.za

https://www.webmed.co.za/medical/topmed-medical-scheme--3165.html

Our business address:-. TopMed Medical Scheme. PO Box 1462. KwaZulu Natal. 4000. Phone : 0860 00 21 58. Fax: 086 762 4050. Send Mail (Contact Us) Visit Our Website vCard.

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healthitanalytics.com

https://healthitanalytics.com/news/precision-medicine-program-analyzes-diverse-genetic-dataset

Feb 15, 2021 . New Tool Could Advance Precision Medicine for Incurable Diseases Called the Trans-Omics for Precision Medicine (TOPMed), the program seeks to understand the genetic variations that occur among individuals in nuclear families and populations from …

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google.com

https://passwords.google.com/

Welcome to your Password Manager. Manage your saved passwords in Android or Chrome. They’re securely stored in your Google Account and available across all your devices. Password Checkup. Check the strength and security of your saved passwords. Find out if they’ve been compromised and get personalized advice when you need it.

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github.com

https://github.com/statgen/topmed_variant_calling

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nih.gov

https://www.nhlbi.nih.gov/science/precision-medicine-activities

The cloud-based platform for tools, applications, and workflows, and it provides secure workspaces to share, store, cross-link, and analyze large sets of data generated from biomedical and behavioral research, such as NHLBI’s Trans-Omics for Precision Medicine …

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ox.ac.uk

https://www.well.ox.ac.uk/~wrayner/tools/

Download the .tgz and extract all .legend files, place them in a directory together with the following script: concatenate-1000GP.zip. and run the script (perl concatenate-1000GP.pl) this will create a file (1000GP_Phase3_combined.legend) suitable for use with the checking program.

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fedhealth.co.za

https://www.fedhealth.co.za/latest-news/fedhealth-topmed-merger-approved-by-council-for-medical-schemes/

We are very pleased to inform you that the Fedhealth and Topmed amalgamation has been approved by the Council for Medical Schemes (CMS), with effect from 1 August 2019. As an exisiting Fedhealth member, your benefit structure will remain unchanged for the current year, since Fedhealth options, benefits and limits and Rules will apply.

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readthedocs.io

https://imputationserver.readthedocs.io/en/latest/getting-started/

Getting started. To use Michigan Imputation Server, a registration is required. We send an activation mail to the provided address. Please follow the instructions in the email to activate your account. If it doesn't arrive, ensure you have entered the correct email address and check your spam folder.

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nih.gov

https://pubmed.ncbi.nlm.nih.gov/33887194/

Whole-genome sequencing (WGS), a powerful tool for detecting novel coding and non-coding disease-causing variants, has largely been applied to clinical diagnosis of inherited disorders. Here we leveraged WGS data in up to 62,653 ethnically diverse participants from the NHLBI Trans-Omics for Precisio …

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