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Questions related from Francesca Ceroni
I have run my DS cDNA libraries on the Bioanalyzer [see the traces attached]. There is a weird small peak near the lower marker peak and I do not know if these libraries are good or not. Can...
26 June 2014 9,362 3 View
I did a two step ds cDNA synthesis starting from 50 ng and 150 ng enriched mRNA. How can I check my cDNA? I do not see peaks at Bioanalyzer, and I am wondering if the material is too low or if it...
13 March 2014 9,662 2 View
Does anybody have or know a protocol to understand how to optimize RNA/random hexames/temperature in ds cDNA synthesis reaction to get a precise fragment size?
21 January 2014 8,187 2 View
Is there any way to control it?
17 January 2014 3,639 5 View
Which is the advantage of performing a paired end sequencing instead of a single read one? I know it gives information for eukaryotic samples about the splicing variants... but for prokaryotes?
17 January 2014 3,490 5 View
I am about to perform RNAseq on E. coli total transcriptome. I am planning to use the Nextera kit so I need to prepare my own cDNA from total RNA. Since the kits for ds cDNA synthesis are crazily...
16 January 2014 7,652 13 View