Transcriptomic RNA sequencing of Euglena gracilis with rRNA depleted
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https://www.ncbi.nlm.nih.gov/sra/SRP515472
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Total RNA for RNA-seq was extracted and ribosomal RNA was removed using specific probes. A strand-specific library was constructed by synthesizing first strand cDNA with random hexamer primer and M-MuLV transcripase (RNase H-) and second strand cDNA with DNA polymerase I and RNase H. The qualified library was sequenced on a Illumia Nova 6000 platform by Novogene (Beijing, China). This transcriptomic RNA sequencing is used for expression analysis of protein-coding genes in nuclear and organellar genomes.
创建时间:
2026-01-01



