Partial bisulfite conversion for unique template sequencing

por Kumar, Vijay, Rosenbaum, Julie, Wang, Zihua, Forcier, Talitha, Ronemus, Michael, Wigler, Michael, Levy, Dan
Publicado 2018

SMASH, a fragmentation and sequencing method for genomic copy number analysis

por Wang, Zihua, Andrews, Peter, Kendall, Jude, Ma, Beicong, Hakker, Inessa, Rodgers, Linda, Ronemus, Michael, Wigler, Michael, Levy, Dan
Publicado 2016

Sharing parental genomes by siblings concordant or discordant for autism

por Wroten, Mathew, Yoon, Seungtai, Andrews, Peter, Yamrom, Boris, Ronemus, Michael, Buja, Andreas, Krieger, Abba M., Levy, Dan, Ye, Kenny, Wigler, Michael, Iossifov, Ivan
Publicado 2023

Reducing INDEL calling errors in whole genome and exome sequencing data

por Fang, Han, Wu, Yiyang, Narzisi, Giuseppe, O’Rawe, Jason A, Barrón, Laura T Jimenez, Rosenbaum, Julie, Ronemus, Michael, Iossifov, Ivan, Schatz, Michael C, Lyon, Gholson J
Publicado 2014

Rates of contributory de novo mutation in high and low-risk autism families

por Yoon, Seungtai, Munoz, Adriana, Yamrom, Boris, Lee, Yoon-ha, Andrews, Peter, Marks, Steven, Wang, Zihua, Reeves, Catherine, Winterkorn, Lara, Krieger, Abba M., Buja, Andreas, Pradhan, Kith, Ronemus, Michael, Baldwin, Kristin K., Levy, Dan, Wigler, Michael, Iossifov, Ivan
Publicado 2021