Constructing a meaningful evolutionary average at the phylogenetic center of mass

por Stone, Eric A, Sidow, Arend
Publicado 2007

Transcription-factor occupancy at HOT regions quantitatively predicts RNA polymerase recruitment in five human cell lines

por Foley, Joseph W, Sidow, Arend
Publicado 2013

The future of sequencing: convergence of intelligent design and market Darwinism

por Greenleaf, William J, Sidow, Arend
Publicado 2014

Molecular phylogeny

por Sidow, Arend, Bowman, Barbara H
Publicado 1992

ABC: software for interactive browsing of genomic multiple sequence alignment data

por Cooper, Gregory M, Singaravelu, Senthil AG, Sidow, Arend
Publicado 2004

HAPDeNovo: a haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data

por Zhou, Xin, Batzoglou, Serafim, Sidow, Arend, Zhang, Lu
Publicado 2018

Assessment of human diploid genome assembly with 10x Linked-Reads data

por Zhang, Lu, Zhou, Xin, Weng, Ziming, Sidow, Arend
Publicado 2019

De novo diploid genome assembly for genome-wide structural variant detection

por Zhang, Lu, Zhou, Xin, Weng, Ziming, Sidow, Arend
Publicado 2019

A haplome alignment and reference sequence of the highly polymorphic Ciona savignyi genome

por Small, Kerrin S, Brudno, Michael, Hill, Matthew M, Sidow, Arend
Publicado 2007

Mammalian Comparative Sequence Analysis of the Agrp Locus

por Kaelin, Christopher B., Cooper, Gregory M., Sidow, Arend, Barsh, Gregory S.
Publicado 2007

Multi-omic tumor data reveal diversity of molecular mechanisms that correlate with survival

por Ramazzotti, Daniele, Lal, Avantika, Wang, Bo, Batzoglou, Serafim, Sidow, Arend
Publicado 2018

De novo mutational signature discovery in tumor genomes using SparseSignatures

por Lal, Avantika, Liu, Keli, Tibshirani, Robert, Sidow, Arend, Ramazzotti, Daniele
Publicado 2021

Aquila enables reference-assisted diploid personal genome assembly and comprehensive variant detection based on linked reads

por Zhou, Xin, Zhang, Lu, Weng, Ziming, Dill, David L., Sidow, Arend
Publicado 2021

Comprehensive genomic characterization of breast tumors with BRCA1 and BRCA2 mutations

por Lal, Avantika, Ramazzotti, Daniele, Weng, Ziming, Liu, Keli, Ford, James M., Sidow, Arend
Publicado 2019

Identification of the Otopetrin Domain, a conserved domain in vertebrate otopetrins and invertebrate otopetrin-like family members

por Hughes, Inna, Binkley, Jonathan, Hurle, Belen, Green, Eric D, Sidow, Arend, Ornitz, David M
Publicado 2008

SHRiMP: Accurate Mapping of Short Color-space Reads

por Rumble, Stephen M., Lacroute, Phil, Dalca, Adrian V., Fiume, Marc, Sidow, Arend, Brudno, Michael
Publicado 2009

Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++

por Davydov, Eugene V., Goode, David L., Sirota, Marina, Cooper, Gregory M., Sidow, Arend, Batzoglou, Serafim
Publicado 2010

Constraint and divergence of global gene expression in the mammalian embryo

por Spies, Noah, Smith, Cheryl L, Rodriguez, Jesse M, Baker, Julie C, Batzoglou, Serafim, Sidow, Arend
Publicado 2015

Determinants of nucleosome organization in primary human cells

por Valouev, Anton, Johnson, Steven M., Boyd, Scott D., Smith, Cheryl L., Fire, Andrew Z., Sidow, Arend
Publicado 2011

Genome-Wide Analysis of Transcription Factor Binding Sites Based on ChIP-Seq Data

por Valouev, Anton, Johnson, David S., Sundquist, Andreas, Medina, Catherine, Anton, Elizabeth, Batzoglou, Serafim, Myers, Richard M., Sidow, Arend
Publicado 2008