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A survey of rare epigenetic variation in 23,116 human gen... | ResearchHub
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A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions
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Authors
Paras Garg
13 more
Paras Garg
•
Bharati Jadhav
11 more
•
Andrew Sharp
Published
March 26, 2020
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Preprint Server
Topics
Biology
Genetics And Genomics
Medicine
Genetics
Epigenetics
Show all topics
DOI
10.1101/2020.03.25.007864
License
cc-no
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Medicine
Genetics
Epigenetics
Show all topics
DOI
10.1101/2020.03.25.007864
License
cc-no
