Using Apache Spark on genome assembly for scalable overlap-graph reduction

por Paul, Alexander J., Lawrence, Dylan, Song, Myoungkyu, Lim, Seung-Hwan, Pan, Chongle, Ahn, Tae-Hyuk
Publicado 2019

Whole-Genome and Long-Read Sequencing Identify a Novel Mechanism in RFC1 Resulting in CANVAS Syndrome

por King, Katherine Abell, Wegner, Daniel J., Bucelli, Robert C., Shapiro, Jessica, Paul, Alexander J., Dickson, Patricia I., Wambach, Jennifer A.
Publicado 2022

LONGO: an R package for interactive gene length dependent analysis for neuronal identity

por McCoy, Matthew J, Paul, Alexander J, Victor, Matheus B, Richner, Michelle, Gabel, Harrison W, Gong, Haijun, Yoo, Andrew S, Ahn, Tae-Hyuk
Publicado 2018

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

por Kobren, Shilpa Nadimpalli, Baldridge, Dustin, Velinder, Matt, Krier, Joel B., LeBlanc, Kimberly, Esteves, Cecilia, Pusey, Barbara N., Züchner, Stephan, Blue, Elizabeth, Lee, Hane, Huang, Alden, Bastarache, Lisa, Bican, Anna, Cogan, Joy, Marwaha, Shruti, Alkelai, Anna, Murdock, David R., Liu, Pengfei, Wegner, Daniel J., Paul, Alexander J., Sunyaev, Shamil R., Kohane, Isaac S.
Publicado 2021