It is with heartfelt congratulations that we share that Dr. Marco Marra has been appointed an Officer of the Order of Canada.
Dr. Marra is recognized for how he “propelled Canada to the forefront of genome research.”
Learn more: https://t.co/rd9nYuQyjf
Mutational signature analysis has become a key tool for interpreting somatic mutations. Our tool MuSiCal (Mutational Signature Calculator) by the amazing Hu Jin (@hujin2hujin2) and Doga Gulhan (@dcgulhan) is out at Nat Genetics: https://t.co/8Cy6dWmhPa. Three key ideas below.
Aneuploidy is a defining feature of cancer cells, but is it also present in healthy normal tissues? In our paper out today on @NatureGenet, we report hundreds of mosaic chromosomal alterations (mCAs) found in diverse tissues from #GTEx. A thread (1/7)
https://t.co/JtzP7d1oRL
@jakelee0711@Nature Many congratulations, Jake! I am so impressed by your dedication and tenacity to decipher these complex rearrangement events to arrive at the causal mechanism. Congratulations again! 👏👏👏
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We are excited to share our new story about how oncogenes are amplified in breast cancer genomes and the role of estrogen in igniting this process through genomic rearrangements. The story came out in @Nature today, and here is the thread!
https://t.co/wTARjKuVPH
We are delighted to be the Data Analysis Center for this new NIH Common Fund effort!
NIH launches $140 million effort to investigate genetic variation in normal human cells and tissues https://t.co/51tbWtMnYZ
Here is a story of how @jinkukkim found an antisense oligonucleotide (ASO) that can up-regulate a key protein in a neurodegenerative disease. Joint work between my lab and @timyu. 1/n https://t.co/18QumKBju7
Congratulations to evolutionary biologist & @ZoolgyUBC prof Dr. Sarah Otto (@sarperotto) on winning a #KillamPrize2023.
@nrc_cnrc#UBC
https://t.co/ffOz4X5G9J
Abstract Select: @peter_j_park from @harvardmed focusing on single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements at the 2023 @AGBT General Meeting. #AGBT23
Can we identify single nucleotide variants and indels accurately at the single cell level? Joe Luquette developed SCAN2 to examine >50 neurons and finds enrichment of indels at brain-specific enhancers/promoters. Collab with @ChrisAWalsh1
lab. Full text: https://t.co/jFIT1vkThE
I am thrilled that our work on predicting PARPi response in breast and ovarian cancers using mutational signatures from panel data is out at @CCR_AACR! Collaborating with @felipe_batalini and Gerburg Wulf was great, and many thanks to @peter_j_park!
👇
https://t.co/phHWIQP19f
Interested in mining #GeneticInteraction and #CoEssential networks from #DepMap? Try out GRETA! It's a simple-to-use R package with options to customize your queries based on mutations, cancer context, and much more.
https://t.co/xTfNdZCMsl
It's here–the deepest, sharpest infrared view of the universe to date: Webb's First Deep Field.
Previewed by @POTUS on July 11, it shows galaxies once invisible to us. The full set of @NASAWebb's first full-color images & data will be revealed July 12: https://t.co/63zxpNDi4I