Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method
出版年份 2013 全文链接
标题
Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method
作者
关键词
Mosaicism, Parent-of-origin, Trio, Parent–child, Software, Microarray, Autism, Cleft, HapMap
出版物
BMC GENOMICS
Volume 14, Issue 1, Pages 367
出版商
Springer Nature
发表日期
2013-06-01
DOI
10.1186/1471-2164-14-367
参考文献
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。- Chromosomal variation in lymphoblastoid cell lines
- (2012) Matthew D. Shirley et al. HUMAN MUTATION
- Detectable clonal mosaicism and its relationship to aging and cancer
- (2012) Kevin B Jacobs et al. NATURE GENETICS
- Detectable clonal mosaicism from birth to old age and its relationship to cancer
- (2012) Cathy C Laurie et al. NATURE GENETICS
- A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data
- (2011) Juan R González et al. BMC BIOINFORMATICS
- Frequent Aneuploidy Among Normal Human Hepatocytes
- (2011) Andrew W. Duncan et al. GASTROENTEROLOGY
- Sensitive quantification of mosaicism using high density SNP arrays and the cumulative distribution function
- (2011) Thomas C. Markello et al. MOLECULAR GENETICS AND METABOLISM
- A Mosaic Activating Mutation inAKT1Associated with the Proteus Syndrome
- (2011) Marjorie J. Lindhurst et al. NEW ENGLAND JOURNAL OF MEDICINE
- GPHMM: an integrated hidden Markov model for identification of copy number alteration and loss of heterozygosity in complex tumor samples using whole genome SNP arrays
- (2011) Ao Li et al. NUCLEIC ACIDS RESEARCH
- Estimation of Parent Specific DNA Copy Number in Tumors using High-Density Genotyping Arrays
- (2011) Hao Chen et al. PLoS Computational Biology
- Inference of Relationships in Population Data Using Identity-by-Descent and Identity-by-State
- (2011) Eric L. Stevens et al. PLoS Genetics
- An integrated Bayesian analysis of LOH and copy number data
- (2010) Paola MV Rancoita et al. BMC BIOINFORMATICS
- Somatic Genome Variations in Health and Disease
- (2010) I. Iourov et al. CURRENT GENOMICS
- Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis
- (2010) Laura K. Conlin et al. HUMAN MOLECULAR GENETICS
- Somatic gene mutation and human disease other than cancer: An update
- (2010) Robert P. Erickson MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
- A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
- (2010) Terri H Beaty et al. NATURE GENETICS
- MixHMM: Inferring Copy Number Variation and Allelic Imbalance Using SNP Arrays and Tumor Samples Mixed with Stromal Cells
- (2010) Zongzhi Liu et al. PLoS One
- Integrated study of copy number states and genotype calls using high-density SNP arrays
- (2009) Wei Sun et al. NUCLEIC ACIDS RESEARCH
- High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians
- (2009) Hajime Matsuzaki et al. GENOME BIOLOGY
- Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios
- (2008) Johan Staaf et al. BMC BIOINFORMATICS
- Aneuploid mosaicism in the developing and adult cerebellar cortex
- (2008) Jurjen W. Westra et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Modeling genetic inheritance of copy number variations
- (2008) Kai Wang et al. NUCLEIC ACIDS RESEARCH
- Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays
- (2008) Johan Staaf et al. GENOME BIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started