Source: https://www.biospace.com/article/releases/nebula-genomics-la...
Source: https://www.biospace.com/article/releases/nebula-genomics-la...
I joined the program a week ago. Did all surveys and I'm currently sitting on 550 credits. To qualify for a their main genome sequencing, "Low-pass Whole Genome Sequencing (0.4x coverage)", you need 1000 credits or $99. But if you want whole genome sequenced, you need to order their flagship product, "Clinical-grade Whole Genome Sequencing (30x coverage)". Which is greyed out on their website currently. And I'm not even going to guess how many credits is that going to cost.
https://us.dantelabs.com/blogs/news/dante-labs-black-friday-...
In addition to the variant containing VCF file, on request they offer the raw read data on hard disk in FASTQ and BAM format (mapped I presume).
Have you had a chance to do so?
which makes me feel better about the (obviously also subsidised by potential research use) $199 full genome Black Friday deal I just ordered...
That's an amazing sequence of words.