I'm not surprised that they moved to subscription. But an annual $5000 buy in to give someone the opportunity to pay to use apps is ridiculous.
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To be fair, that $5k (if that is what the cost of the mid-tier subscription is) appears to include two additional features.Originally posted by thermophile View PostI'm not surprised that they moved to subscription. But an annual $5000 buy in to give someone the opportunity to pay to use apps is ridiculous.
Whether "Multi-user access" and 8hr of bioinformatics professional services support is worth $5K, is open to debate
If you don't have any local IT infrastructure then that may be your sole option.
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Software release note for 2.18 has this listed as "known issue"Originally posted by kcchan View PostThat issue still hasn't been fixed as of the the most recent 2.18 update.
“N” is incorrectly allowed as an index sequence character in the sample sheet. When used, this will cause a mismatch for any sequence character other than “N”.
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Does that apply to all apps or just the third party ones that we would normally be paying for? Right now, it looks like the usual basic analyses I'm used to running are still accessible from a basic account, but I think my account is still on a trial basis from the changeover.Originally posted by kcchan View PostI would imagine some of the third party developers aren't too happy either since their apps are now stuck behind a paywall.
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Wait, so we can't even do FastQC with a free account? I was able to run it, but like I said yesterday, my account is still in trial mode. Are you just trying to use the Illumina/BaseSpace Labs 16s metagenomics app? I'm not hopeful for my Amplicon DS analyses, then....Originally posted by thermophile View PostI can select a sample, launch FastQC or 16S metagenomics, but then I don't have the start button
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Jessica, I can't run any apps at all. My understanding is that every new account gets a 30day trial so I guess you could just make a new email and account every month to continue using the apps.Microbial ecologist, running a sequencing core. I have lots of strong opinions on how to survey communities, pretty sure some are even correct.
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While that may work short term, it may land you on Illumina's blacklist (if they watch for what IP's the accounts are logging in from).Originally posted by thermophile View PostJessica, I can't run any apps at all. My understanding is that every new account gets a 30day trial so I guess you could just make a new email and account every month to continue using the apps.
Small cores may need to adjust their prices (and account for $5K subscription) if they find BaseSpace indispensable for daily business.
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True. I'm likely going to go back to ignoring the basespace apps and use it just for fastq distribution which is still currently feasible for my miseq only core on a free account.Originally posted by GenoMax View PostWhile that may work short term, it may land you on Illumina's blacklist (if they watch for what IP's the accounts are logging in from).
Small cores may need to adjust their prices (and account for $5K subscription) if they find BaseSpace indispensable for daily business.Microbial ecologist, running a sequencing core. I have lots of strong opinions on how to survey communities, pretty sure some are even correct.
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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Channel: Articles
07-01-2026, 11:43 AM -
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by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
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