Hi all,
    I have a question regarding to DEseq differential expression analysis.
    In DEseq, is there any way to detect whether the library from one sample
is totally screwed up?
    Or for signal gene, the expression is abnormal in one sample (For this
situation, do we just abandon this value or modify it)?
Thanks!
best,
Laurie


-- 
Rui Luo
Lab phone : 310 794-7537
Geschwind Lab
Human Genetics Department
UCLA

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