But isn't it essential to know how the data was generated and what kind of biases one should expect?
The term third party library prep kit means it is compatible with a certain sequencer (e.g. NextSeq or IonProton) but was not provided by the sequencer's company.
Fair point, that's essential, but then a lot more things become essential as well and we can also discuss pure biology, biochemistry, enzymatic reactions etc here, with on the other side server architecture and pure programming. But the scope of Biostars is to discuss bioinformatics.
Hi all, Regarding stranded-specific library preparation by dUTP method, as far as I know, the dUTP is used during the synthesis of the second strand, …
<p>Hi all,</p> <p>I have a basic question, so sorry in advance. I'm getting a bit confused about "hit length" in the blast output (ncbi-blast-2.2.30+). Please …
Hi all, I have separately done several blasx of a assembled transcriptome against some proteome organism as tabular format (`-outfmt 6`). Now I would like …
This is not really bioinformatics, is it? Do we even come in before the sequencing data is ready?
But isn't it essential to know how the data was generated and what kind of biases one should expect?
The term third party library prep kit means it is compatible with a certain sequencer (e.g. NextSeq or IonProton) but was not provided by the sequencer's company.
Fair point, that's essential, but then a lot more things become essential as well and we can also discuss pure biology, biochemistry, enzymatic reactions etc here, with on the other side server architecture and pure programming. But the scope of Biostars is to discuss bioinformatics.
Hello seta!
We believe that this post does not fit the main topic of this site.
Not related to bioinformatics, more appropriate for seqanswers (but already answered here now so eh)
For this reason we have closed your question. This allows us to keep the site focused on the topics that the community can help with.
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