相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions
Dario G. Lupianez et al.
CELL (2015)
CRISPR Inversion of CTCF Sites Alters Genome Topology and Enhancer/Promoter Function
Ya Guo et al.
CELL (2015)
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development
Gwang-Jin Kim et al.
JOURNAL OF MEDICAL GENETICS (2015)
The SOX9 upstream region prone to chromosomal aberrations causing campomelic dysplasia contains multiple cartilage enhancers
Baojin Yao et al.
NUCLEIC ACIDS RESEARCH (2015)
Chromatin extrusion explains key features of loop and domain formation in wild-type and engineered genomes
Adrian L. Sanborn et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice
Katerina Kraft et al.
CELL REPORTS (2015)
Functional Assessment of Disease-Associated Regulatory Variants In Vivo Using a Versatile Dual Colour Transgenesis Strategy in Zebrafish
Shipra Bhatia et al.
PLOS GENETICS (2015)
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
Suhas S. P. Rao et al.
CELL (2014)
Functional and topological characteristics of mammalian regulatory domains
Orsolya Symmons et al.
GENOME RESEARCH (2014)
Identification of Novel Craniofacial Regulatory Domains Located far Upstream of SOX9 and Disrupted in Pierre Robin Sequence
Christopher T. Gordon et al.
HUMAN MUTATION (2014)
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Michael I. Love et al.
GENOME BIOLOGY (2014)
STAR: ultrafast universal RNA-seq aligner
Alexander Dobin et al.
BIOINFORMATICS (2013)
Exploring long-range genome interactions using the WashU Epigenome Browser
Xin Zhou et al.
NATURE METHODS (2013)
Copy-number changes in evolution: rates, fitness effects and adaptive significance
Vaishali Katju et al.
Frontiers in Genetics (2013)
An inwardly rectifying K+ channel is required for patterning
Giri Raj Dahal et al.
DEVELOPMENT (2012)
Topological domains in mammalian genomes identified by analysis of chromatin interactions
Jesse R. Dixon et al.
NATURE (2012)
Spatial partitioning of the regulatory landscape of the X-inactivation centre
Elphege P. Nora et al.
NATURE (2012)
Fast gapped-read alignment with Bowtie 2
Ben Langmead et al.
NATURE METHODS (2012)
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development
Sabina Benko et al.
JOURNAL OF MEDICAL GENETICS (2011)
Large-scale analysis of the regulatory architecture of the mouse genome with a transposon-associated sensor
Sandra Ruf et al.
NATURE GENETICS (2011)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
The brachydactylies: a molecular disease family
S. Mundlos
CLINICAL GENETICS (2009)
Long-range regulation at the SOX9 locus in development and disease
C. T. Gordon et al.
JOURNAL OF MEDICAL GENETICS (2009)
Complex landscapes of somatic rearrangement in human breast cancer genomes
Philip J. Stephens et al.
NATURE (2009)
Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia
Ingo Kurth et al.
NATURE GENETICS (2009)
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
Sabina Benko et al.
NATURE GENETICS (2009)
Sex determination involves synergistic action of SRY and SF1 on a specific Sox9 enhancer
Ryohei Sekido et al.
NATURE (2008)
Genomic rearrangements and sporadic disease
James R. Lupski
NATURE GENETICS (2007)
VISTA Enhancer Browser - a database of tissue-specific human enhancers
Axel Visel et al.
NUCLEIC ACIDS RESEARCH (2007)
分享论文
