Hi all,
I have been receiving some confusing output with an RNA-seq dataset that I am trying to ultimately determine differential expression...
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RNA-Seq Library Prep in 2-Hours!?
BioDynami has launched the fastest RNA-Seq library prep kit in the market. With our technology, you can easily make high quality RNA-Seq libraries in...
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Two cDNA Peaks on Bioanalyzer
I used 200 ng total RNA input and the KAPA HyperPrep Kit to generate cDNA libraries. Usually, our libraries look like Sample 1 in the attached pdf, but...
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Scriptseq complete gold epidem
I have total RNA extracted from environmental samples that I intend to sequence. The main aim is to detect viral and bacterial transcripts.
...
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Ransom Library prep for GC-rich genes
Hi,
We would like to do differential expression analysis, we did a genome (Illumina + PacBIo) and a transcriptome (Kapa mRNA kit) but GC-rich genes...
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adapter contamination in reads?????
hello everyone,
I would like to ask one qus: why am I getting 3'adapter sequences in R1 and R2 reads (as according to seq...
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How much DNA contamination "allowed"?
Hi,
We're going to do a RNA-SEQ experiment (with Nextseq 500) with bacterial RNA for differential gene expression. We have cells lysed...
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De novo Transcriptome and size selection
Hello,
I would like to have your opinion on this:
Would it help me for the my transcriptome assembly if I first made a size selection during...
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TruSeq PCR Prep Box - DNA/RNA
Hi all,
I wonder is there any difference between TruSeq DNA PCR Prep Box and TruSeq DNA PCR Prep Box?
Looks like we accidentally...Last edited by MLog; 10-28-2012, 03:39 AM.
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Adventures in cluster density titration.
We have perennial issues with obtaining sane/consistent library concentrations prior to clustering. Those of you with a HiSeq will probably have this...
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RNA-seq libraries - double peak after size selection
Hi everyone,
I get some weird results when measuring my RNA-seq libraries on Bioanalyzer and now desperately need an advice...
The libraries...Last edited by MLog; 02-08-2012, 02:46 PM.