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ExomeSeqData
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Database for exploring annotations of the coding genome at variants, such as candidate regulatory SNPs at disease-associated loci.
SNP
ExomeSeqData
snapcount
SNAData
SNPRelate
7 months ago
m610110001
• 0
1 result • Page
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Comment: Handling NA's in Deseq2
by
Asger Mølgaard
• 0
Dear ATpoint Thank you for your response - it works like a charm! You just saved a PhD-study! Thank you :)
Comment: Ensembl plants at annotationHub?
by
Bruno
• 0
Hi Guido, Thanks for your fast reply the error was as said in my question "Annotation must be a GRanges object", when I tried to use the a…
Comment: Ensembl plants at annotationHub?
by
Guido Hooiveld
★ 3.6k
You did not show the code that resulted in that error, so we have to guess what you did. Yet, the [R package][1] `Signac` contains the func…
Comment: Query regarding phyloseq object construct with QIIME output
by
betterwound
• 0
Thanks for sharing the code [geometry dash](https://geometrydash.io/)
Answer: Ensembl plants at annotationHub?
by
Bruno
• 0
Hi Johannes, First, thank you so much for providing these annotations for the community. We feel often a bit left off in the plant commu…
Votes
C: Minimum number of samples per treatment/group for WGCNA analysis
A: Minimum number of samples per treatment/group for WGCNA analysis
Minimum number of samples per treatment/group for WGCNA analysis
Comment: DESeq2 on multilevel design variable
Comment: Ensembl plants at annotationHub?
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