We've updated the AllSeq NGS Knowledge Bank to reflect the latest Illumina instruments - all the specs in one place!
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Updated Illumina Specs Table
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Can the 2500 Rapid mode really produce 600M clusters in the two 'lanes'? I've seen results more along 150-180M clusters. Maybe I'm thinking of passing filters and this table is not, but I don't think I've seen the lanes loaded to make 300M clusters each either.Providing nextRAD genotyping and PacBio sequencing services. http://snpsaurus.com
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I can't say for sure, but that's the spec for two flow cells (and the number of reads needed to generate the claimed 180Gb per run). Those could be pre-filtered reads, but I wouldn't think filtering would cut the # of reads by half. Hopefully others can chime in with their real world results.Originally posted by SNPsaurus View PostCan the 2500 Rapid mode really produce 600M clusters in the two 'lanes'? I've seen results more along 150-180M clusters. Maybe I'm thinking of passing filters and this table is not, but I don't think I've seen the lanes loaded to make 300M clusters each either.
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Ahh, 600M X 300 bp = 180 Gb, so that would be 150M clusters per lane x 2 reads x 150 bp. I think you are counting clusters in some columns and total reads possible (2 per cluster) in others.Providing nextRAD genotyping and PacBio sequencing services. http://snpsaurus.com
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Remember that Illumina stats are always in Run output assuming you are running with as many flow cells as possible. A HiSeq 2500 can output 600M clusters per Run which means (150M clusters per lane) X (2 lanes per flow cell) X (2 flow cells per run).Originally posted by SNPsaurus View PostCan the 2500 Rapid mode really produce 600M clusters in the two 'lanes'? I've seen results more along 150-180M clusters. Maybe I'm thinking of passing filters and this table is not, but I don't think I've seen the lanes loaded to make 300M clusters each either.
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In all cases the stated outputs should be for entire runs (both flow cells for two flow cell machines). All reads -should- be single reads/clusters. If you find examples where we screwed that up, please let me know and we'll fix it ASAP.Originally posted by SNPsaurus View PostAhh, 600M X 300 bp = 180 Gb, so that would be 150M clusters per lane x 2 reads x 150 bp. I think you are counting clusters in some columns and total reads possible (2 per cluster) in others.
For the HiSeq 2500 Rapid Mode we have:
2 flow cells X 300M reads/flow cell X 2x150bp reads
2*300M*2*150b=180Gb
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Right, sorry for the confusion. The single flow cell NextSeq got me messed up going back to the two-flow-cell HiSeq.Providing nextRAD genotyping and PacBio sequencing services. http://snpsaurus.com
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I agree that it gets kind of confusing - that's why we built the tableOriginally posted by SNPsaurus View PostRight, sorry for the confusion. The single flow cell NextSeq got me messed up going back to the two-flow-cell HiSeq.
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by SEQadmin2
NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...-
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by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
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