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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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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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Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...-
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Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...-
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