The TOPMed Whole Genome Sequencing data are available in dbGaP. Researchers can apply for access (2/n)

https://www.ncbi.nlm.nih.gov/gap/ 
The TOPMed variant catalog can be found at
the bravo website maintained at the University of Michigan (3/n)

https://bravo.sph.umich.edu/freeze8/hg38/ 
The multi-faceted functional annotations of the TOPMed variants can be found at http://favor.genohub.org  (4/n)
The TOPMed imputation server can be found at
…https://imputation.biodatacatalyst.nhlbi.nih.gov/# ! (5/n)
More detailed information about TOPMed can be found at https://www.nhlbiwgs.org/  (6/n)
Great thread by @gabecasis about the @nature TOPMed paper. Thanks for his, UW TOPMed Data Coordinating Center, and NHLBI, and many TOPMed investigators' leadership and contributions to the TOPMed Nature paper. https://twitter.com/gabecasis/status/1359706729219575810
You can follow @XihongLin.
Tip: mention @twtextapp on a Twitter thread with the keyword “unroll” to get a link to it.

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