Recurrent Somatic Mutations in Regulatory Regions of Human Cancer Genomes

por Melton, Collin, Reuter, Jason A., Spacek, Damek V., Snyder, Michael
Publicado 2015

Simul-seq: combined DNA and RNA sequencing for whole-genome and transcriptome profiling

por Reuter, Jason A, Spacek, Damek V, Pai, Reetesh K, Snyder, Michael P
Publicado 2016

The wooly mutation (wly) on mouse chromosome 11 is associated with a genetic defect in Fam83g

por Radden, Legairre A, Child, Kevin M, Adkins, Elisabeth B, Spacek, Damek V, Feliciano, Aaron M, King, Thomas R
Publicado 2013

Phenotypic characteristics of peripheral immune cells of Myalgic encephalomyelitis/chronic fatigue syndrome via transmission electron microscopy: A pilot study

por Jahanbani, Fereshteh, Maynard, Rajan D., Sing, Justin Cyril, Jahanbani, Shaghayegh, Perrino, John J., Spacek, Damek V., Davis, Ronald W., Snyder, Michael P.
Publicado 2022

Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans

por Cenik, Can, Cenik, Elif Sarinay, Byeon, Gun W., Grubert, Fabian, Candille, Sophie I., Spacek, Damek, Alsallakh, Bilal, Tilgner, Hagen, Araya, Carlos L., Tang, Hua, Ricci, Emiliano, Snyder, Michael P.
Publicado 2015

The juvenile alopecia mutation (jal) maps to mouse Chromosome 2, and is an allele of GATA binding protein 3 (Gata3)

por Ramirez, Francisco, Feliciano, Aaron M, Adkins, Elisabeth B, Child, Kevin M, Radden II, Legairre A, Salas, Alexis, Vila-Santana, Nelson, Horák, José M, Hughes, Samantha R, Spacek, Damek V, King, Thomas R
Publicado 2013

Landscape of cohesin-mediated chromatin loops in the human genome

por Grubert, Fabian, Srivas, Rohith, Spacek, Damek  V, Kasowski, Maya, Ruiz-Velasco, Mariana, Sinnott-Armstrong, Nasa, Greenside, Peyton, Narasimha, Anil, Liu, Qing, Geller, Benjamin, Sanghi, Akshay, Kulik, Michael, Sa, Silin, Rabinovitch, Marlene, Kundaje, Anshul, Dalton, Stephen, Zaugg, Judith B., Snyder, Michael
Publicado 2020