Aaron Quinlan, PhD

Affiliations: 
1997 College of William and Mary, Williamsburg, VA 
 2008 Boston College, Newton, MA, United States 
 2008-2015 University of Virginia, Charlottesville, VA 
 2015- Human Genetics University of Utah, Salt Lake City, UT 
Website:
http://quinlanlab.org/
Google:
"Aaron Quinlan"
Mean distance: (not calculated yet)
 

Parents

Sign in to add mentor
Gabor T. Marth grad student 2008 Boston College
Ira M. Hall post-doc 2008-2011 UVA
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Chamberlin JT, Gillen AE, Quinlan AR. (2024) Improved characterization of 3' single-cell RNA-seq libraries with paired-end avidity sequencing. Nar Genomics and Bioinformatics. 6: lqae175
Thorpe HJ, Pedersen BS, Dietze M, et al. (2024) Identification of as a genetic modifier of PIGA-CDG through pedigree analysis of a family with incomplete penetrance and functional testing in . Biorxiv : the Preprint Server For Biology
Porubsky D, Dashnow H, Sasani TA, et al. (2024) A familial, telomere-to-telomere reference for human mutation and recombination from a four-generation pedigree. Biorxiv : the Preprint Server For Biology
Chamberlin JT, Gillen AE, Quinlan AR. (2024) Improved characterization of single-cell RNA-seq libraries with paired-end avidity sequencing. Biorxiv : the Preprint Server For Biology
Chamberlin JT, Lee Y, Marth G, et al. (2024) Differences in molecular sampling and data processing explain variation among single-cell and single-nucleus RNA-seq experiments. Genome Research
Hou H, Pedersen B, Quinlan A. (2024) Author Correction: Balancing efficient analysis and storage of quantitative genomics data with the D4 format and d4tools. Nature Computational Science. 2: 132
Dolzhenko E, English A, Dashnow H, et al. (2024) Characterization and visualization of tandem repeats at genome scale. Nature Biotechnology
Khan MR, Akbari A, Nicholas TJ, et al. (2023) Genome sequencing of Pakistani families with male infertility identifies deleterious genotypes in SPAG6, CCDC9, TKTL1, TUBA3C, and M1AP. Andrology
Dashnow H, Pedersen BS, Hiatt L, et al. (2022) STRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel loci. Genome Biology. 23: 257
Goldstein SA, Brown J, Pedersen BS, et al. (2022) Extensive Recombination-driven Coronavirus Diversification Expands the Pool of Potential Pandemic Pathogens. Genome Biology and Evolution. 14
See more...