Update: Are you studying #genomic variants and looking for a method that provides #eQTL, #chromatin looping, #epigenetic mark, #TF binding sites, and other data? 🧬 Let's dive in! https://t.co/92fTamNyoE
Are you studying genomic variants and looking for a method that provides eQTL, chromatin looping, epigenetic mark, TF binding sites, and other data? Check out the new FORGEdb web tool https://t.co/bhrnzTMNLJ
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Our understanding of disease variants in minorities is hampered by the fact that many epigenomic datasets are not available for certain populations. How to tackle this problem? Find out about our work with @NoraFranceschi2 just out @NatureGenet!
https://t.co/6Di5JqFAyk
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A Resource paper from @aetesch, @charles_breeze and colleagues presents a DNA methylation atlas that can be used for in silico cell-type deconvolution of human tissues.
OA paper: https://t.co/NsW3EhLzIx
Our understanding of cell-type-specific processes in disease development is hampered by the fact that bulk-tissue DNA methylomes are an average of many diverse cell types. How to tackle this problem? Find out about our most recent work with @aetesch just out @naturemethods!
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