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Maybe another application could be the ranking of candidate variants for cancer immunotherapy? As far as I know, lncRNAs are sometimes assessed.


We haven't looked into this deeply yet sounds interesting. Do you have any resources where to start looking at this? Feel free to reach out to us

founders@blankbio.com


Yes, most bioinformatics tools are the result of research projects.

However, the most common bioinformatics file formats have actually been devised by excellent software engineers (e.g. SAM/BAM, VCF, BED).

I think it is just very convenient to have text-based formats as you don't need any special libraries to read/modify the files and can reach for basic Unix text-processing tools instead. Such modifications are often needed in a research context.

Also, space-efficient file formats (e.g. CRAM) are often within reach once disk space becomes a pressing issue. Now you only need to convince the team to use them. :)


Unfortunately the line between 2 and 3 is very blurry. Like paper mill output submitted to legimate medium-to-low impact journals. Some of it gets inevitably published, others just puts a strain on peer reviewers.


An alternative for the use case of spawning dev environments would be https://github.com/pvolok/mprocs


I have no 23&Me profile, and I prefer to keep my genome private. However, IF you are NOT in the personal-data risk-averse camp, there is a point in rather giving your genome data than giving your online activity profiles. The former can at least be used for biology research/treatment development and thus clearly has higher upside for humanity.


I generally enjoyed the article. Maybe it's because the classical functional categorization/cataloging approaches in molecular biology are rarely sufficient to explain experimental data unless you are an expert and know all the exceptions and special cases. So the Predictive Biology approach seems a promising path, particularly since a lot of data for ML training is available.

That said, the formulation "machine learning is the native language of biology" seems odd.


I agree with the low demand for more expensive personal WGS. I think you can mostly get what you want with ySeq: currently 400$ for 90 GigaBases WGS sequencing, with the data sent to you via SD card. You can request immediate data deletion. Only genealogical analysis is included, everything else is DIY.


Thanks for the tip on ySeq.

I think there is some sort of middle ground here. Although 99% of consumers don't care about privacy, it's an org risk as we saw with 23&Me. A consumer focused, privacy heavy but cloud based platform will emerge in the wake of 23&Me.


ySeq has a 5 month waiting list for WGS, any other suggestions?


what would you pay for this service? how quickly would you want the data? what format do you want the data in?


399 from YSeq seems fine for 30x coverage.

Gemini says a reasonable cost estimate from saliva to SNPs is $163.84 - $211.84 using Ultima $80 for sequencing (funny that sequencing is no longer the bottleneck on cost).

FASTQ is fine but I'd prefer BINSEQ: https://github.com/ArcInstitute/binseq. I'm writing my own pipeline from BINSEQ.


I wonder if letting guinea pigs listen to Adele's 'I Miss You' at 102 dB for long periods required approval from an ethics council.


Maybe the poor things had depression after that and it impacted their behavior.


I find that the Airbnb fees are too high for what you get, which often boils down to the contact information of the renter. For some regions in Europe, I actually prefer again local vacation rental agencies, which have similar fees but much more service. Of course, their websites are often not great, but describing your requirements via phone or email gives great options.


Related discussion from 2 months ago: https://news.ycombinator.com/item?id=43403821


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