Comparison of phylogenetic trees through alignment of embedded evolutionary distances

por Choi, Kwangbom, Gomez, Shawn M
Publicado 2009

A Bayesian mixture model for the analysis of allelic expression in single cells

por Choi, Kwangbom, Raghupathy, Narayanan, Churchill, Gary A.
Publicado 2019

Bayesian model selection reveals biological origins of zero inflation in single-cell transcriptomics

por Choi, Kwangbom, Chen, Yang, Skelly, Daniel A., Churchill, Gary A.
Publicado 2020

Publisher Correction: Bayesian model selection reveals biological origins of zero inflation in single-cell transcriptomics

por Choi, Kwangbom, Chen, Yang, Skelly, Daniel A., Churchill, Gary A.
Publicado 2020

Airpart: interpretable statistical models for analyzing allelic imbalance in single-cell datasets

por Mu, Wancen, Sarkar, Hirak, Srivastava, Avi, Choi, Kwangbom, Patro, Rob, Love, Michael I
Publicado 2022

PRDM9 Drives Evolutionary Erosion of Hotspots in Mus musculus through Haplotype-Specific Initiation of Meiotic Recombination

por Baker, Christopher L., Kajita, Shimpei, Walker, Michael, Saxl, Ruth L., Raghupathy, Narayanan, Choi, Kwangbom, Petkov, Petko M., Paigen, Kenneth
Publicado 2015

Natural genetic variation determines microglia heterogeneity in wild-derived mouse models of Alzheimer’s disease

por Yang, Hongtian Stanley, Onos, Kristen D., Choi, Kwangbom, Keezer, Kelly J., Skelly, Daniel A., Carter, Gregory W., Howell, Gareth R.
Publicado 2021

SEESAW: detecting isoform-level allelic imbalance accounting for inferential uncertainty

por Wu, Euphy Y., Singh, Noor P., Choi, Kwangbom, Zakeri, Mohsen, Vincent, Matthew, Churchill, Gary A., Ackert-Bicknell, Cheryl L., Patro, Rob, Love, Michael I.
Publicado 2023

Affinity-seq detects genome-wide PRDM9 binding sites and reveals the impact of prior chromatin modifications on mammalian recombination hotspot usage

por Walker, Michael, Billings, Timothy, Baker, Christopher L., Powers, Natalie, Tian, Hui, Saxl, Ruth L., Choi, Kwangbom, Hibbs, Matthew A., Carter, Gregory W., Handel, Mary Ann, Paigen, Kenneth, Petkov, Petko M.
Publicado 2015

RNA-Seq Alignment to Individualized Genomes Improves Transcript Abundance Estimates in Multiparent Populations

por Munger, Steven C., Raghupathy, Narayanan, Choi, Kwangbom, Simons, Allen K., Gatti, Daniel M., Hinerfeld, Douglas A., Svenson, Karen L., Keller, Mark P., Attie, Alan D., Hibbs, Matthew A., Graber, Joel H., Chesler, Elissa J., Churchill, Gary A.
Publicado 2014

Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment

por Kemp, John P., Medina-Gomez, Carolina, Estrada, Karol, St Pourcain, Beate, Heppe, Denise H. M., Warrington, Nicole M., Oei, Ling, Ring, Susan M., Kruithof, Claudia J., Timpson, Nicholas J., Wolber, Lisa E., Reppe, Sjur, Gautvik, Kaare, Grundberg, Elin, Ge, Bing, van der Eerden, Bram, van de Peppel, Jeroen, Hibbs, Matthew A., Ackert-Bicknell, Cheryl L., Choi, Kwangbom, Koller, Daniel L., Econs, Michael J., Williams, Frances M. K., Foroud, Tatiana, Carola Zillikens, M., Ohlsson, Claes, Hofman, Albert, Uitterlinden, André G., Davey Smith, George, Jaddoe, Vincent W. V., Tobias, Jonathan H., Rivadeneira, Fernando, Evans, David M.
Publicado 2014