Tuuli Lappalainen

@tuuliel

Group leader at NY Genome Center & Columbia University, studying functional variation in the human genome.

New York City, NY, USA
tllab.org
Menyertai Mei 2012
67 Foto atau video 67 Foto dan video Foto dan video

Tweet

Anda telah menyekat @tuuliel

Adakah anda pasti anda mahu melihat Tweet ini? Melihat Tweet tidak akan menyekat @tuuliel

  1. Mengetweet Semula
    2 jam lalu

    This is a huge piece of work on pooled screen for 204 human cell lines from 12 cancer types targeting 18,009 genes for cellular fitness genes -> 6,830 gene loss of fitness -> > 500 core fitness genes => 497 priority genes. In short huge dataset

    1 balasan1 balasan 21 tweet semula21 tweet semula 44 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  2. Mengetweet Semula
    2 jam lalu

    Could gene-centic functional screens be valuable for functional follow up of results, in addition to the numerous variant-centric approaches being employed? Our preprint applying this approach for blood trait GWAS is posted: (1/2)

    2 balasan2 balasan 6 tweet semula6 tweet semula 8 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  3. Mengetweet Semula
    5 jam lalu

    Data imitates decorations. One view is of James Hotel across Sixth Avenue, the other a screen on fourth floor of

    3 balasan3 balasan 2 tweet semula2 tweet semula 10 suka
    Buat asal
  4. Mengetweet Semula
    7 jam lalu

    From abstract of new : "We show that trait associated loci cover more than half of the genome, and 90% of those loci are associated with multiple trait domains." Me: 😮😮🤔. Very cool -- check it out here:

    12 tweet semula12 tweet semula 26 suka
    Buat asal
  5. 8 jam lalu

    Exceptions include my department's pre-award team and others who help me to get $$$

    1 balasan1 balasan 4 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  6. 10 jam lalu

    PSA: Any company/vendor/institute that emails me a holiday greetings will be blocked.

    2 balasan2 balasan 18 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  7. Mengetweet Semula
    22 jam lalu

    Our new paper: Using Equivalent Class counts directly for testing differential transcript usage. Nice work from

    6 balasan6 balasan 35 tweet semula35 tweet semula 76 suka
    Buat asal
  8. Mengetweet Semula
    19 Dis

    Our paper on high-resolution mapping of driver nucleotides in transcriptional regulatory elements is out today! This work from the and labs came together at the very end of my Ph.D. (1/5)

    3 balasan3 balasan 56 tweet semula56 tweet semula 128 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  9. Mengetweet Semula
    19 Dis

    Me for on the case for Bernie Sanders in 2020:

    21 balasan21 balasan 45 tweet semula45 tweet semula 172 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  10. Mengetweet Semula
    19 Dis

    Our Cell Hashing work w/ is out ! Check out a few awesome experimental approaches for scRNA-seq multiplexing: - () - (Gartner Lab) - () -

    1 balasan1 balasan 79 tweet semula79 tweet semula 169 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  11. 19 Dis

    Donations by NYers until 12/31 will be matched 6x, so even small $ now for make a big difference! She's endorsed by e.g. and . Special election will be in February. 2/2

    1 balasan1 balasan 1 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  12. 19 Dis

    I donated to support campaign for NYC Public Advocate - our watchdog against corruption. She's an activist, journalist, a fierce progressive fighter. Don't take my word, watch this: and donate in 1/2

    1 balasan1 balasan 1 tweet semula1 tweet semula 4 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  13. Mengetweet Semula
    17 Dis

    Inferring Compensatory Evolution of cis- and trans-Regulatory Variation

    1 balasan1 balasan 24 tweet semula24 tweet semula 65 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  14. Mengetweet Semula
    17 Dis

    A great issue on human evolutionary genetics edited by Brenna Henn () and myself. Great reviews by great people. Thanks to all. Enjoy it. Current Opinion in Genetics & Development | Genetics of Human Origins |

    2 balasan2 balasan 61 tweet semula61 tweet semula 109 suka
    Buat asal
  15. 18 Dis

    Congratulations ! Based on productivity during only 5 weeks of postdoc work here, I expect to celebrate more achievements in not too distant future!

    Today we celebrated passing her PhD viva with minor corrections. Feeling very proud of your achievements. Congratulations Dafni, well done! Big day for Dafni, big day for the group!
    16 suka
    Buat asal
  16. Mengetweet Semula
    16 Dis

    WRITING A PAPER IN WORD: FONT TIPS Contrary to widely held belief (among LaTeX fands), it is easy to write a nice-looking paper in Word. You just have to do three things: (1) use styles; (2) avoid hideous fonts; (3) unleash the fonts’ potential. 2\

    11 balasan11 balasan 175 tweet semula175 tweet semula 556 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  17. Mengetweet Semula
    18 Dis

    New from the lab. We identified trans- in stimulated /macrophages including risk allele in CLU and MS4A loci influencing distal expression of type 1 , complement and myeloid genes.

    Tensor Decomposition of Stimulated Monocyte and Macrophage Gene Expression Profiles Identifies Neurodegenerative Disease-specific Trans-eQTLs
    1 balasan1 balasan 20 tweet semula20 tweet semula 31 suka
    Tunjukkan thread ini
    Tunjukkan thread ini
    Buat asal
  18. Mengetweet Semula
    18 Dis

    Super excited about our work! A new set test method for association testing using summary statistics.

    Leveraging allelic heterogeneity to increase power of association testing
    1 balasan1 balasan 17 tweet semula17 tweet semula 31 suka
    Buat asal
  19. 17 Dis

    Looking for advice: our project looks at phenomena across diverse GWAS traits and environmental factors. Is it OK to just apply access to all the data (looks like a lot of clicking though) since we don't know which fields we'll need - or do I need to be more specific?

    4 balasan4 balasan 6 tweet semula6 tweet semula 10 suka
    Buat asal
  20. Mengetweet Semula
    17 Dis

    Where to go for rare disease diagnoses after exome sequencing fails? Excellent review of the options by and :

    2 balasan2 balasan 121 tweet semula121 tweet semula 191 suka
    Buat asal

@tuuliel belum lagi Tweet.

Pemuatan nampaknya mengambil sedikit masa.

Twitter mungkin melebihi kapasiti atau mengalami gangguan seketika. Cuba sekali lagi atau lawati Status Twitter untuk mendapatkan maklumat lanjut.

    Anda juga mungkin menyukai

    ·