3 ms·

There are telomeres and centromeres on the ends and middle of chromosomes that have really long repeating sequences, which until recently were hard to sequence.

by ece 5y ago

There are telomeres and centromeres on the ends and middle of chromosomes that have really long repeating sequences, which until recently were hard to sequence. This sequenced those long sequences, from a fertilized egg that apparently didn't have any female DNA. Next steps are sequencing more individuals. If this sequencing tech gets cheap enough, individualized medicine could take a big leap forward. I hope that's a good summary. https://www.washingtonpost.com/science/2022/03/31/human-genome-complete/ https://www.washingtonpost.com/science/2022/03/31/human-geno...

ma2t 5y ago
Has no male DNA (no Y chromosome), and is completely homozygous which simplified the assembly. https://web.expasy.org/cellosaurus/CVCL_VU12 https://web.expasy.org/cellosaurus/CVCL_VU12
- ece 5y ago
  The cell was female, but due to a quirk, the DNA was all male? Or I'm not understanding what the WaPo article said. The genome does have a Y chromosome: https://www.ncbi.nlm.nih.gov/assembly/GCA_009914755.4#/def https://www.ncbi.nlm.nih.gov/assembly/GCA_009914755.4#/def
  - ma2t 5y ago
    That Y chromosome was added by applying same analysis workflow to a different biological source (CORIELL:NA24385, a NIST standard material used in the Genome in a Bottle project). The other chromosomes are all from the CHM13htert line (if you click on the individual chromosomes at your link above, you can scroll down to the "/isolate" feature to see what material the sequence was derived from). There's a long tradition of having a reference assembly be a combination of different individuals. Even the "standard" GRCh38/hg38 reference doesn't represent any single individual.
    - ece 4y ago
      Thanks for that explanation. I wonder how much harder it'll be to sequence a heterozygous genome.
robwwilliams 4y ago
First part true. Second part is doubtful. Individualized medicine needs a much more robust computational framework than it current has. Each of us has a unique genome, a unique developmental history, and has lived in a unique environment. We are n=1 experiments. Organ culture and IPSCs are a pipe dream. Here is our approach to addressing this barrier: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979527/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979527/

by ece 5y ago

ma2t 5y ago

Has no male DNA (no Y chromosome), and is completely homozygous which simplified the assembly. https://web.expasy.org/cellosaurus/CVCL_VU12 https://web.expasy.org/cellosaurus/CVCL_VU12

ece 5y ago
The cell was female, but due to a quirk, the DNA was all male? Or I'm not understanding what the WaPo article said. The genome does have a Y chromosome: https://www.ncbi.nlm.nih.gov/assembly/GCA_009914755.4#/def https://www.ncbi.nlm.nih.gov/assembly/GCA_009914755.4#/def
- ma2t 5y ago
  That Y chromosome was added by applying same analysis workflow to a different biological source (CORIELL:NA24385, a NIST standard material used in the Genome in a Bottle project). The other chromosomes are all from the CHM13htert line (if you click on the individual chromosomes at your link above, you can scroll down to the "/isolate" feature to see what material the sequence was derived from). There's a long tradition of having a reference assembly be a combination of different individuals. Even the "standard" GRCh38/hg38 reference doesn't represent any single individual.
  - ece 4y ago
    Thanks for that explanation. I wonder how much harder it'll be to sequence a heterozygous genome.

robwwilliams 4y ago

First part true. Second part is doubtful. Individualized medicine needs a much more robust computational framework than it current has. Each of us has a unique genome, a unique developmental history, and has lived in a unique environment. We are n=1 experiments. Organ culture and IPSCs are a pipe dream. Here is our approach to addressing this barrier: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979527/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979527/