Mystery of Somerton man’s identity solved after 73 years, researchers say - https://news.ycombinator.com/item?id=32251717 - July 2022 (14 comments)
Australia Exhumes the Somerton Man, and His 70-Year Mystery - https://news.ycombinator.com/item?id=27250937 - May 2021 (5 comments)
The Lost Man - https://news.ycombinator.com/item?id=9666581 - June 2015 (4 comments)
The Body on Somerton Beach (2011) - https://news.ycombinator.com/item?id=7913942 - June 2014 (14 comments)
But the epilogue about how being an electronics engineer gave them a bit of a unique edge feels like a self-serving stretch. The techniques in the story seem accessible to any reasonably well-learned individual if they’re motivated enough to sleuth. All the advanced work was done by other people. And there’s a tinge of the classic, “the established discipline is living in the past but us engineers can do it better…”
> What’s interesting about solving such a case is how it relies on concepts that may seem counterintuitive to forensic biologists but are quite straightforward to an electronics engineer.
They're only claiming it's "counterintuitive" to biologists trained in other methods.
Imagine a forensinc lab using imputation to identify some samples and arresting someone based on them. It takes only a slighly interested lawyer to destroy that evidence at trial, saying that imputation is, literally, making up a good amount of data. In fact, defendant lawyers put a lot of effort in invalidating evidence, and imputation is quite easy to attack.
This case is a good sample to build upon it, to try to introduce imputation as a victim identification. But forensics move slowly.
It's a classic for a reason :)
No more successful relationships or sinister ways of ensuring genetic survival are required.
What does this mean? SNPs being, by definition, single nucleotide polymorphisms, how does the author jump from 1bp to 50-150bp? Or is he referring to the surrounding DNA region?
[1]: https://en.wikipedia.org/wiki/Single-nucleotide_polymorphism
But that's not a SNP, then, that's a read that happens to contain a SNP.
Generally a SNP is addressed by giving the reference base, the mutated base, the chromosome, the base position in that chromosome, and the assembly used to align the read to that location. For example, a T->C mutation at chr2:25164877 using hg38.
Yes, you need to have the whole read to align to your genome assembly to detect the SNP. But before you do that, you don't know whether you have a SNP. And after you do that, the rest of the read is not useful if what you care about is the SNP.
From the context of the article it's pretty clear that the author was talking about the fragment sizes needed for analysis.
I have a graduate degree in bioinformatics and have worked in the industry for close to a decade, I have a strong background in the exact topic, yes.
Alternately, they're talking about their sequencing reads and calling them SNPs.
I think I should just chalk this one up to my own personal Gell-Mann amnesia and let the article authors do their thing.
One year ago: https://www.youtube.com/watch?v=DCDOYDNZUMI 7 months ago: https://www.youtube.com/watch?v=ve_JrmYsU0I
> In 1949, a pathologist had found a bit of paper concealed in one of the dead man’s pockets, and on it were printed the words Tamám Shud, the Persian for “finished.”
Mistakes are still make quite regularly. Most people (all?) still can't grabs what "confidence interval" or "probability" are.