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Can't find any literature that says anything other than the Nextseq uses 2 colors. In fact, isn't this why the Nextseq currently has GC problems? Haven't heard anything about that with the HiseqX...Originally posted by Brian Bushnell View PostExcept that I'm pretty sure the X-series do use 2-dye chemistry, the same as NextSeq...
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This http://blog.illumina.com/blog/illumi...eq-4000-system says the 4000 uses 4-color.
This http://www.illumina.com/content/dam/...0-2014-057.pdf says that 1 flowcell does 50 transcriptomes per run at 50M reads each, so that is >300M reads per lane. Looks faster as well, if the longest run time is 3.5 days (not sure if that would be for 1x150bp or 2x150bp).Providing nextRAD genotyping and PacBio sequencing services. http://snpsaurus.com
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Heard from someone that the cluster and reagent kits are similar in price to current Hiseq 2000 reagents, which would mean the price per read is quite a bit lower.Providing nextRAD genotyping and PacBio sequencing services. http://snpsaurus.com
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#SNPsaurus:
I assume it will be 2x 150 bp in 3.5 days.
2.1 to 2.5 billion clusters per flow cell, in a 2x150 bp run is 630 - 750 Gb.
With a speed >200Gb per day a 2x 150 bp run will take 3.5 days.
I wonder if we can upgrade the 2500 V4 machine to a 4000 version...
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Ditto. I think supporting the patterned flow-cells would require too much of a reworking of the guts...Originally posted by GenoMax View PostPossible upgrade path for current 2500 owners?
I am not going to hold my breath though.
Seems like they are following the Apple product release model...
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CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).
Despite this, “CRISPR helped turn genome editing from a specialized technique into...-
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