DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism
Authors
Keywords
-
Journal
BIOINFORMATICS
Volume 28, Issue 12, Pages i154-i162
Publisher
Oxford University Press (OUP)
Online
2012-06-11
DOI
10.1093/bioinformatics/bts234
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The Clark Phaseable Sample Size Problem: Long-Range Phasing and Loss of Heterozygosity in GWAS
- (2011) Bjarni V. HalldóRsson et al. JOURNAL OF COMPUTATIONAL BIOLOGY
- An Algorithm for Detecting High Frequency Copy Number Polymorphisms Using SNP Arrays
- (2011) Bjarni V. Halldórsson et al. JOURNAL OF COMPUTATIONAL BIOLOGY
- Mapping copy number variation by population-scale genome sequencing
- (2011) Ryan E. Mills et al. NATURE
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
- (2011) Stephan J. Sanders et al. NEURON
- Genetic Heterogeneity in Human Disease
- (2010) Jon McClellan et al. CELL
- Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
- (2010) Hansoo Park et al. NATURE GENETICS
- Dissecting the Clinical Heterogeneity of Autism Spectrum Disorders through Defined Genotypes
- (2010) Hilgo Bruining et al. PLoS One
- Parent-Of-Origin Effects in Autism Identified through Genome-Wide Linkage Analysis of 16,000 SNPs
- (2010) Delphine Fradin et al. PLoS One
- Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
- (2009) Audrey Guilmatre et al. ARCHIVES OF GENERAL PSYCHIATRY
- Targeted interrogation of copy number variation using SCIMMkit
- (2009) Troy Zerr et al. BIOINFORMATICS
- Duplication hotspots, rare genomic disorders, and common disease
- (2009) Heather C Mefford et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- Origins and functional impact of copy number variation in the human genome
- (2009) Donald F. Conrad et al. NATURE
- Computational methods for discovering structural variation with next-generation sequencing
- (2009) Paul Medvedev et al. NATURE METHODS
- A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
- (2008) Dan E. Arking et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Autism and Brain Development
- (2008) Christopher A. Walsh et al. CELL
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- 1000 Genomes project
- (2008) Nayanah Siva NATURE BIOTECHNOLOGY
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
- Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry
- (2008) E. M. Morrow et al. SCIENCE
- A note on the problem of reporting maximal cliques
- (2008) F. Cazals et al. THEORETICAL COMPUTER SCIENCE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now