Hi there
I want to ask if someone compared data from BGI Illumina 50bp single end RNA-seq, where they use an optimized Illumina protocol for libraries preparation, with same kind of data (samples) obtained from other facilities where they use the TruSeq kit for libraries.
Are those quite comparable or they present strong differences in term of gene expression??
Thanks
I want to ask if someone compared data from BGI Illumina 50bp single end RNA-seq, where they use an optimized Illumina protocol for libraries preparation, with same kind of data (samples) obtained from other facilities where they use the TruSeq kit for libraries.
Are those quite comparable or they present strong differences in term of gene expression??
Thanks
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