scholarly journals QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

2007 ◽  
Vol 35 (6) ◽  
pp. 2013-2025 ◽  
Author(s):  
Stefano Colella ◽  
Christopher Yau ◽  
Jennifer M. Taylor ◽  
Ghazala Mirza ◽  
Helen Butler ◽  
...  
Keyword(s):  
Copy Number Variation ◽  
Markov Model ◽  
Hidden Markov Model ◽  
Copy Number ◽  
Hidden Markov ◽  
Snp Genotyping ◽  
Objective Bayes ◽  
Number Variation

Combinatorial Detection Algorithm for Copy Number Variations Using High-throughput Sequencing Reads

2019 ◽  
Vol 33 (14) ◽  
pp. 1950022
Author(s):  
Hai Yang ◽  
Daming Zhu
Keyword(s):  
Markov Model ◽  
Hidden Markov Model ◽  
High Throughput ◽  
Copy Number ◽  
High Throughput Sequencing ◽  
Hidden Markov ◽  
Read Depth ◽  
Detection Algorithm ◽  
Gc Bias ◽  
Unmapped Reads

Copy number variation (CNV) is a prevalent kind of genetic structural variation which leads to an abnormal number of copies of large genomic regions, such as gain or loss of DNA segments larger than 1[Formula: see text]kb. CNV exists not only in human genome but also in plant genome. Current researches have testified that CNV is associated with many complex diseases. In this paper, guanine-cytosine (GC) bias, mappability and their effect on read depth signals in sequencing data are discussed first. Subsequently, a new correction method for GC bias and an improved combinatorial detection algorithm for CNV using high-throughput sequencing reads based on hidden Markov model (CNV-HMM) are proposed. The corrected read depth signals have lower correlation with GC content, mappability of reads and the width of analysis window. Then we create a hidden Markov model which maps the reads onto the reference genome and records the unmapped reads. The unmapped reads are counted and normalized. The CNV-HMM detects the abnormal signal of read count and gains the candidate CNVs using the expectation maximization (EM) algorithm. Finally, we filter the candidate CNVs using split reads to promote the performance of our algorithm. The experiment result indicates that the CNV-HMM algorithm has higher accuracy and sensitivity for CNVs detection than most current detection algorithms.

scholarly journals hsegHMM: Hidden Markov Model-based Allele-specific Copy Number Alteration Analysis Accounting for Hypersegmentation

2018 ◽  
Author(s):  
Hyoyoung Choo-Wosoba ◽  
Paul S Albert ◽  
Bin Zhu
Keyword(s):  
Markov Model ◽  
Hidden Markov Model ◽  
Copy Number ◽  
Hidden Markov ◽  
Current Method ◽  
Cancer Genome ◽  
The Cancer Genome Atlas ◽  
Cancer Etiology ◽  
Allele Specific ◽  
T Distribution

AbstractBackground:Somatic copy number alternation (SCNA) is a common feature of the cancer genome and is associated with cancer etiology and prognosis. The allele-specific SCNA analysis of a tumor sample aims to identify the allele-specific copy numbers of both alleles, adjusting for the ploidy and the tumor purity. Next generation sequencing platforms produce abundant read counts at the base-pair resolution across the exome or whole genome which is susceptible to hypersegmentation, a phenomenon where numerous regions with very short length are falsely identified as SCNA.Results:We propose hsegHMM, a hidden Markov model approach that accounts for hypersegmentation for allele-specific SCNA analysis. hsegHMM provides statistical inference of copy number profiles by using an effcient E-M algorithm procedure. Through simulation and application studies, we found that hsegHMM handles hypersegmentation effectively with a t-distribution as a part of the emission probability distribution structure and a carefully defined state space. We also compared hsegHMM with FACETS which is a current method for allele-specific SCNA analysis. For the application, we use a renal cell carcinoma sample from The Cancer Genome Atlas (TCGA) study.Conclusions:We demonstrate the robustness of hsegHMM to hypersegmentation. Furthermore, hsegHMM provides the quantification of uncertainty in identifying allele-specific SCNAs over the entire chromosomes. hsegHMM performs better than FACETS when read depth (coverage) is uneven across the genome.

Genome-wide characteristics of copy number variation in Polish Holstein and Polish Red cattle using SNP genotyping assay

Genetica ◽  
2015 ◽  
Vol 143 (2) ◽  
pp. 145-155 ◽  
Author(s):  
A. Gurgul ◽  
I. Jasielczuk ◽  
T. Szmatoła ◽  
K. Pawlina ◽  
T. Ząbek ◽  
...  
Keyword(s):  
Copy Number Variation ◽  
Copy Number ◽  
Snp Genotyping ◽  
Genotyping Assay ◽  
Genome Wide ◽  
Number Variation

scholarly journals HaplotypeCN: Copy Number Haplotype Inference with Hidden Markov Model and Localized Haplotype Clustering

PLoS ONE ◽  
2014 ◽  
Vol 9 (5) ◽  
pp. e96841 ◽  
Author(s):  
Yen-Jen Lin ◽  
Yu-Tin Chen ◽  
Shu-Ni Hsu ◽  
Chien-Hua Peng ◽  
Chuan-Yi Tang ◽  
...  
Keyword(s):  
Markov Model ◽  
Hidden Markov Model ◽  
Copy Number ◽  
Hidden Markov ◽  
Haplotype Inference

scholarly journals Comparison of Normalization Methods for Defining Copy Number Variation Using Whole-genome SNP Genotyping Data

2008 ◽  
Vol 6 (4) ◽  
pp. 231-234 ◽  
Author(s):  
Ji-Hong Kim ◽  
Seon-Hee Yim ◽  
Yong-Bok Jeong ◽  
Seong-Hyun Jung ◽  
Hai-Dong Xu ◽  
...  
Keyword(s):  
Copy Number Variation ◽  
Copy Number ◽  
Snp Genotyping ◽  
Whole Genome ◽  
Normalization Methods ◽  
Number Variation
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