Study linking depression to specific altered brain cells opens door to new treatments mcgill.ca/newsroom/chann… via @mcgillu
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Anjali Chawla
18 posts
Anjali Chawla
@TrippyNeuron
PhD candidate in Neuroscience, McGill University. #HBHL #DKG #FRQS fellowship recipient. Studying #epigenetics in the human brain at single-cell resolution.
Katılım Temmuz 2021
43 Takip Edilen40 Takipçiler
Anjali Chawla retweetledi
@McLeanHospital @harvardmed @_brainstorm_12 @mcgillu @McGill_VPRI @SustainMcGill 💬 Now onto our first panel session, which focuses on how we respond to trauma. Experts from @mcgillu and beyond share their research on traumatic brain injury, stigma, pandemic stress and more. 🧠🤕
#HBHLSymposium2024 @trippyneuron @disastrousmj @carmenlogie @UofT @UofT_FIFSW
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What are the long-term impacts of trauma? How can it cause depression? How can we try to answer these questions through DNA sequencing of brain cells? Please join me for my talk on May 8th @HBHLMcGill hbhlsymposium.ca/speakers/ Register: eventbrite.ca/e/hbhl-symposi…
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Anjali Chawla retweetledi
Curious about what awaits you at #HBHLSymposium2024? 👩🔬🧠
Check out hbhlsymposium.ca/speakers/ to learn more about our exciting line-up of keynotes and panelists, from @mcgillu's brain health community and beyond! 🌎
Don't miss out, register now: eventbrite.ca/e/hbhl-symposi…
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Anjali Chawla retweetledi
Anjali Chawla retweetledi
Summary of 6 statistical methods that can be used for A/B Testing (and when to use them). 🧵
#DataScience #Rstats #Python
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@SingleCellClubM @TheNeuro_MNI @LabStratton @easchurr @LanglaisLab I will be discussing peak calling, clustering, annotation, snATAC-seq and snRNA-seq integration, stratified LDSC, and causal variant identification.
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@SingleCellClubM @TheNeuro_MNI @LabStratton @easchurr @LanglaisLab Hi there, please sign up to join me for a discussion on techniques and application of snATAC-seq integrated with snRNA-seq for major depressive disorder.
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Anjali Chawla retweetledi
Dear SC community
Join us on Nov 29th, 9am EST for Anjali Chawla @TrippyNeuron talk on integrated analysis of snRNA-seq and snATAC-seq in major depressive disorder. Zoom link available via our website singlecellclub.ca.
@TheNeuro_MNI @LabStratton @easchurr @LanglaisLab
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Anjali Chawla retweetledi
#QuartoTipOfTheDay
💪 So Simple.
🔥 So powerful!
➡️ Make ANY ggplot2 chart interactive with 1️⃣ line of code 😱 !
Your report will be so much better!
productive-r-workflow.com/quarto-tricks
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Anjali Chawla retweetledi
Differential Chromatin Architecture and Risk Variants in Deep Layer Excitatory Neurons and Grey Matter Microglia Contribute to Major ... biorxiv.org/cgi/content/sh… #biorxiv_genomic
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Anjali Chawla retweetledi
I am very proud of this work in collaboration with Gustavo Turecki, driven by the brilliant @MalosreeM and supported by @TrippyNeuron, Naguib Mechawar and many others @DouglasResearch
Nature Mental Health@NatMentHealth
🔥Hot off the press @NatureComms: @DrCorinaNagy et al. show concordant cortical transcriptomic patterns in #depression within individual cell types in males and females, although major dysregulated cell types and genes were distinct for each sex.♂️♀️ 👇 nature.com/articles/s4146…
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Anjali Chawla retweetledi
Anjali Chawla retweetledi
Anjali Chawla sharing the aims of her study on "Cell-type specific open #chromatin signatures in the brains of individuals diagnosed with major depressive disorder and died by suicide."
#CanEpi21 #ThisIsEpigenetics
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Tune-in for my talk on Nov. 5th at the 7th Annual Canadian Conference on Epigenetics. The talk will be directly related to my PhD research on - "Cell-type specific open chromatin in the brains of individuals diagnosed with the major depressive disorder"
twitter.com/CEEHRC/status/…
Canadian Epigenetics@CEEHRC
Registration is OPEN! The 7th Canadian Conference on Epigenetics is November 2 to 5, 2021 with both in-person (at Estérel, Quebec) & virtual attendance options. Visit ceehrc.ca/2021 for confirmed speakers & info on registration, travel awards & abstract submission
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Anjali Chawla retweetledi
This article reviews the #chromatin research in disease occurrences, elucidating how non-coding genetic variations impact complex diseases. Congratulations to the authors!
More info: mdpi.com/1422-0067/22/1…
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