Lukas Habegger, Ph.D.

Yale University, New Haven, CT 
Computational Biology and Bioinformatics
"Lukas Habegger"


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Mark B. Gerstein grad student 2012 Yale
 (Computational Methodologies for Transcript Analysis in the Age of Next-Generation DNA Sequencing.)
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Sun KY, Bai X, Chen S, et al. (2024) A deep catalogue of protein-coding variation in 983,578 individuals. Nature
Ziyatdinov A, Torres J, Alegre-Díaz J, et al. (2023) Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature
Sun KY, Bai X, Chen S, et al. (2023) A deep catalog of protein-coding variation in 985,830 individuals. Biorxiv : the Preprint Server For Biology
Backman JD, Li AH, Marcketta A, et al. (2021) Exome sequencing and analysis of 454,787 UK Biobank participants. Nature
Van Hout CV, Tachmazidou I, Backman JD, et al. (2020) Exome sequencing and characterization of 49,960 individuals in the UK Biobank. Nature
Martin CL, Wain KE, Oetjens MT, et al. (2020) Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population. Jama Psychiatry
Staples J, Maxwell EK, Gosalia N, et al. (2018) Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes. American Journal of Human Genetics. 102: 874-889
Dewey FE, Murray MF, Overton JD, et al. (2016) Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study. Science (New York, N.Y.). 354
Packer JS, Maxwell EK, O'Dushlaine C, et al. (2015) CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data. Bioinformatics (Oxford, England)
Abyzov A, Iskow R, Gokcumen O, et al. (2013) Analysis of variable retroduplications in human populations suggests coupling of retrotransposition to cell division. Genome Research. 23: 2042-52
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