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  4. September 2020

News

New preprint on exome imputation and fine-mapping in UK Biobank

September 01, 2020
We are excited to share a new preprint, "Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses" (Barton et al.), which reports an atlas of 1,189...
Read More New preprint on exome imputation and fine-mapping in UK Biobank

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Latest News

  • Nolan Kamitaki and Simone Rubinacci join the lab!

    January 26, 2023

    Nolan is a graduate student in the HMS Bioinformatics and Integrative Genomics (BIG) PhD program and Simone is a postdoctoral fellow at BWH / HMS. We are very excited that they have joined the lab...

    Read More Nolan Kamitaki and Simone Rubinacci join the lab!
  • Maxwell Sherman receives his PhD

    November 18, 2022
    Maxwell Sherman has completed MIT's Electrical Engineering and Computer Science (EECS) PhD program and is moving on to Serinus Biosciences, which he co-founded earlier this year. Congratulations, Max!
  • Paper on haplotype-informed CNV detection published in Cell

    October 27, 2022
    Margaux Hujoel's paper on haplotype-informed CNV detection (HI-CNV; Hujoel et al. 2022 Cell) is now published -- congratulations, Margaux! This work explores the phenotypic impact of rare copy number...
    Read More Paper on haplotype-informed CNV detection published in Cell
  • New preprint on repeat polymorphisms influencing glaucoma and colorectal cancer risk

    October 14, 2022
    We are excited to share a new preprint, "Repeat polymorphisms in non-coding DNA underlie top genetic risk loci for glaucoma and colorectal cancer" (Mukamel*, Handsaker* et al.), which identifies...
    Read More New preprint on repeat polymorphisms influencing glaucoma and colorectal cancer risk
  • Two platform talks at ASHG 2022

    August 31, 2022

    We're very excited to share our latest work at ASHG this October! Ronen Mukamel and Margaux Hujoel will present platform talks describing strong associations of structural variants with heritable...

    Read More Two platform talks at ASHG 2022
  • Paper on cancer mutation modeling published in Nature Biotechnology

    June 20, 2022
    Maxwell Sherman's paper on modeling somatic mutation rates to uncover cancer drivers (Sherman*, Yaari*, Priebe* et al. 2022 Nat Biotech) is now published -- congratulations, Max! This work, a...
    Read More Paper on cancer mutation modeling published in Nature Biotechnology
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