Assistant professor at Dartmouth College. PhD@Yale, PostDoc@UChicago. Disease genetics, genomics, statistical genetics, data science. We are hiring! She/her.

Hanover, New Hamphire
Joined October 2017
My department at Dartmouth is hiring! Senior faculty positions broadly in the field of biostatistics, with a focus on cancer.
Tenured or tenure-track biostatistics faculty position at the rank of Associate or Full Professor available @BioMedDataSci and Dartmouth Cancer Center (@DartmouthCancer) at Dartmouth’s Geisel School of Medicine (@GeiselMed)! Learn more and apply here 👉 apply.interfolio.com/158241
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We then applied our method to a few commonly studied traits (IBD, SBP, schizophrenia) and revealed novel candidate genes. Below is an example of a novel candidate gene (UBE2W) cTWAS identified for IBD, whose association falls below standard TWAS cutoff. 5/n
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When applying cTWAS on real data, it identified much fewer genes than TWAS, the majority of the TWAS false positive findings were due to confounding by nearby causal variants. 6/n
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Our software is available at github.com/xinhe-lab/ctwas. Many thanks to my postdoc advisors @xinhe @mstephens999 co-first author @wescrouse, Sheng Qian and Kevin Luo! Please try our R package and let us know your feedback. Thanks! n/n.
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cTWAS solves this problem by including **all** nearby genes and variants in a Bayesian fine-mapping model, which effectively let gene and variant effects compete to explain the association signal. cTWAS has a well calibrated FPR, without much loss in power. 4/n
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nearby causal variants or eQTLs of causal genes of the trait can be correlated with the gene under test, thus serving as confounders in the test and resulting in false positives (FP). In simulations, we show previous methods can be severely inflated with FP ( FPR > 50%). 3/n
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Many methods have been developed to leverage eQTLs to nominate candidate genes of complex traits, including TWAS, colocalization, mendelian randomization (MR) based methods, etc. However, they all suffer from a key problem: 2/n
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I missed tweeting this when posted in Dec. Our attempt to ameliorate some problems with confounding in TWAS. Key idea is to compete (imputed) gene expression and SNPs against one another as explanations for an asssocation. biorxiv.org/content/10.1101/…
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Molecular & Systems Biology at the Geisel School of Medicine at Dartmouth is excited to recruit Assistant/Associate Professors to our department. Find information on the breadth of our search and our commitment to faculty diversity at geiselmed.dartmouth.edu/msb/… @GeiselMed @Dartmouth
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The University of Chicago, Department of Human Genetics, is searching for a new computational faculty. apply.interfolio.com/112673 We are a small, friendly department doing top-quality science. Come join us! (Please RT)
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Rockefeller's president Richard Lifton, who pioneered the use of genomics to identify the basis for diseases, has been announced as the 2023 recipient of the George M. Kober Medal from the Association of American Physicians. Congratulations! rockefeller.edu/news/32155-r…
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Out now from @Joans and me - (nearly) everything you know about survival analysis in cancer is wrong. cell.com/cell-reports/fullte…
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registration still open for upcoming workshop on eliciting structure in genomics data imsi.institute/eliciting-str… Aug 30-Sept 3. Great line up of speakers. Come join us by zoom!
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I am looking for postdocs !Please RT
Post-doctoral Scholar in Biomedical Data Science with @SimingZhao06 Dartmouth College, Hanover, New Hamphire, USA jobrxiv.org/job/dartmouth-co… #ScienceJobs
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Siming Zhao retweeted
Post-doctoral Scholar in Biomedical Data Science with @SimingZhao06 Dartmouth College, Hanover, New Hamphire, USA jobrxiv.org/job/dartmouth-co… #ScienceJobs
I am beyond excited to say that I just started my lab at Dartmouth college. More details from the lab website (simingzhaolab.org/).
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We will be working with genomics data to decipher the genetic etiology of human diseases, in particular cancer. We are actively hiring, if you are interested in joining us, shoot me an email.
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Check out our new paper on allele-specific open chromatin QTLs! We provide comprehensive genetic analysis for these variants in human iPSC differentiated neuronal cells. The importance of this class of variants is indicated by its enrichment for risk alleles in brain disorders.
This Post is from an account that no longer exists. Learn more
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@xinhe2 @jubao9812 , thanks for letting me involved in this great collaborated project.
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