home.social

#sequencing — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #sequencing, aggregated by home.social.

  1. After more than two weeks, the Grauniad now has an #obituary for #CraigVenter: theguardian.com/science/2026/m I was kind of surprised that he died at a normal age, rather than using his resources to engineer his own immortality.

    #science #genome #DNA #sequencing #humanGenome

  2. After more than two weeks, the Grauniad now has an #obituary for #CraigVenter: theguardian.com/science/2026/m I was kind of surprised that he died at a normal age, rather than using his resources to engineer his own immortality.

    #science #genome #DNA #sequencing #humanGenome

  3. After more than two weeks, the Grauniad now has an #obituary for #CraigVenter: theguardian.com/science/2026/m I was kind of surprised that he died at a normal age, rather than using his resources to engineer his own immortality.

    #science #genome #DNA #sequencing #humanGenome

  4. After more than two weeks, the Grauniad now has an #obituary for #CraigVenter: theguardian.com/science/2026/m I was kind of surprised that he died at a normal age, rather than using his resources to engineer his own immortality.

    #science #genome #DNA #sequencing #humanGenome

  5. After more than two weeks, the Grauniad now has an #obituary for #CraigVenter: theguardian.com/science/2026/m I was kind of surprised that he died at a normal age, rather than using his resources to engineer his own immortality.

    #science #genome #DNA #sequencing #humanGenome

  6. Speaking of - anyone know if there's any documentation/literature on how ONT put together their bacterial dorado polishing model?

    I know it fares well in benchmarks, but curious about non-bacterial prokaryotes. Is anyone putting together their own polishing models for test?

    #bioinformatics #sequencing #ONT

  7. Speaking of - anyone know if there's any documentation/literature on how ONT put together their bacterial dorado polishing model?

    I know it fares well in benchmarks, but curious about non-bacterial prokaryotes. Is anyone putting together their own polishing models for test?

    #bioinformatics #sequencing #ONT

  8. Speaking of - anyone know if there's any documentation/literature on how ONT put together their bacterial dorado polishing model?

    I know it fares well in benchmarks, but curious about non-bacterial prokaryotes. Is anyone putting together their own polishing models for test?

    #bioinformatics #sequencing #ONT

  9. Speaking of - anyone know if there's any documentation/literature on how ONT put together their bacterial dorado polishing model?

    I know it fares well in benchmarks, but curious about non-bacterial prokaryotes. Is anyone putting together their own polishing models for test?

    #bioinformatics #sequencing #ONT

  10. Speaking of - anyone know if there's any documentation/literature on how ONT put together their bacterial dorado polishing model?

    I know it fares well in benchmarks, but curious about non-bacterial prokaryotes. Is anyone putting together their own polishing models for test?

    #bioinformatics #sequencing #ONT

  11. Single-molecule #peptide #sequencing through reverse translation of peptides into DNA
    nature.com/articles/s41587-026

    everything that can be bound with/converted to DNA can be "sequenced": it's sort of like SBS, but here DNA oligos are used instead of individual DNA bases and later actual SBS is performed to decode each oligo sequence... every read will inform about single aa at single position from single protein.
    to sequence a protein with 300 aa, you'll need to sequence at least 300 reads!
    neat!

  12. Single-molecule #peptide #sequencing through reverse translation of peptides into DNA
    nature.com/articles/s41587-026

    everything that can be bound with/converted to DNA can be "sequenced": it's sort of like SBS, but here DNA oligos are used instead of individual DNA bases and later actual SBS is performed to decode each oligo sequence... every read will inform about single aa at single position from single protein.
    to sequence a protein with 300 aa, you'll need to sequence at least 300 reads!
    neat!

  13. Single-molecule #peptide #sequencing through reverse translation of peptides into DNA
    nature.com/articles/s41587-026

    everything that can be bound with/converted to DNA can be "sequenced": it's sort of like SBS, but here DNA oligos are used instead of individual DNA bases and later actual SBS is performed to decode each oligo sequence... every read will inform about single aa at single position from single protein.
    to sequence a protein with 300 aa, you'll need to sequence at least 300 reads!
    neat!

  14. Single-molecule #peptide #sequencing through reverse translation of peptides into DNA
    nature.com/articles/s41587-026

    everything that can be bound with/converted to DNA can be "sequenced": it's sort of like SBS, but here DNA oligos are used instead of individual DNA bases and later actual SBS is performed to decode each oligo sequence... every read will inform about single aa at single position from single protein.
    to sequence a protein with 300 aa, you'll need to sequence at least 300 reads!
    neat!

  15. Single-molecule #peptide #sequencing through reverse translation of peptides into DNA
    nature.com/articles/s41587-026

    everything that can be bound with/converted to DNA can be "sequenced": it's sort of like SBS, but here DNA oligos are used instead of individual DNA bases and later actual SBS is performed to decode each oligo sequence... every read will inform about single aa at single position from single protein.
    to sequence a protein with 300 aa, you'll need to sequence at least 300 reads!
    neat!

  16. RE: genomic.social/@jfy133/1160918

    🚨 LAST CHANCE! 🚨

    🧬 Do you work with #sequencing data, and have a spare 5 minutes to help contribute to making #genomics #metadata standards more #FAIR?|

    🎰 Want a chance to win a little prize pack?

    💡 Reminder of the our @NFDI4Microbiota and Genomic Standards Consortium funded survey (link below)!

    📅 Deadline is 20th March (end of tomorrow!)!

  17. How can #epigenetic modifications of #DNA be studied to better understand #biology?

    In her talk at #Biochemistry2026, Sabine Schneider talked about her group's exciting work on developing new TET3 enzymes that improve epigenetic sequencing.

    pubs.rsc.org/en/content/articl
    #Chemistry #Biochemistry #ChemBio #Sequencing
    CC: @gdch, @GDCh_BioChem

  18. Yoga Sequencing: Designing Transformative Yoga Classes "A comprehensive, timely, and much-needed work on the important art of sequencing" Sale: $24.95 to $1.99 by Mark Stephens Rating: 4.8/5 (2,358 Reviews) #Yoga #Sequencing #Teaching #Asana #Wellness #BookSky

    Yoga Sequencing: Designing Tra...

  19. Yoga Sequencing: Designing Transformative Yoga Classes "A comprehensive, timely, and much-needed work on the important art of sequencing" Sale: $24.95 to $1.99 by Mark Stephens Rating: 4.8/5 (2,358 Reviews) #Yoga #Sequencing #Teaching #Asana #Wellness #BookSky

    Yoga Sequencing: Designing Tra...

  20. Yoga Sequencing: Designing Transformative Yoga Classes "A comprehensive, timely, and much-needed work on the important art of sequencing" Sale: $24.95 to $1.99 by Mark Stephens Rating: 4.8/5 (2,358 Reviews) #Yoga #Sequencing #Teaching #Asana #Wellness #BookSky

    Yoga Sequencing: Designing Tra...

  21. Yoga Sequencing: Designing Transformative Yoga Classes "A comprehensive, timely, and much-needed work on the important art of sequencing" Sale: $24.95 to $1.99 by Mark Stephens Rating: 4.8/5 (2,358 Reviews) #Yoga #Sequencing #Teaching #Asana #Wellness #BookSky

    Yoga Sequencing: Designing Tra...

  22. RE: genomic.social/@jfy133/1160918

    😤 Do you work with #sequencing data, and find it frustrating to fill in #metadata to make your data more #FAIR ?

    💡 Reminder of the survey on #genomics metadata standards below!
    📅 Deadline on the 20th March!
    🎰 We have a raffle to win a little prize pack

  23. #Linux tools for examining #sequencing data:

    ```
    zcat sequences.fastq.gz | \
    awk 'NR % 4 == 2 { print substr($0, 0, 10) }' |\
    sort | uniq -c | sort -nr > index_list
    ```

    Generates a list of the first 10 bases in sequences.fastq.gz, sorted by frequency. Handy if you need to check that the indexes you thought you used are in fact the ones that were used.

    ```
    $ head index_list
    10765621 ACGTACTGTG
    9006389 AACCACGCTT
    6891089 ACACCGTTGC
    5198342 AGAAGCCATT
    4202651 AATCGAGGTG
    3788448 ACCTTGTGCA
    3271929 ACGAGTTGCA
    3027755 ACCGATTGCA
    2682797 ACTATCCGTG
    54372 ACGTANTGTG
    ...
    ```

    This may become a blogpost at some point.

    #bioinformatics