Buki G, Hadzsiev K, Bene J
Int J Mol Sci. 2023; 24(18).
PMID: 37761973
PMC: 10530736.
DOI: 10.3390/ijms241813671.
Muller G, de Godoy V, Dario M, Duval E, Alves-Jr S, Bucker A
J Fungi (Basel). 2023; 9(8).
PMID: 37623574
PMC: 10456111.
DOI: 10.3390/jof9080803.
Barbitoff Y, Matveenko A, Matiiv A, Maksiutenko E, Moskalenko S, Drozdova P
G3 (Bethesda). 2021; 11(4).
PMID: 33677552
PMC: 8759820.
DOI: 10.1093/g3journal/jkab029.
AlShibli A, Mathkour H
Saudi J Biol Sci. 2020; 27(12):3647-3654.
PMID: 33304176
PMC: 7714972.
DOI: 10.1016/j.sjbs.2020.08.007.
Nakatochi M, Kushima I, Ozaki N
J Hum Genet. 2020; 66(1):25-37.
PMID: 32958875
DOI: 10.1038/s10038-020-00838-1.
Genomic region detection via Spatial Convex Clustering.
Nagorski J, Allen G
PLoS One. 2018; 13(9):e0203007.
PMID: 30204756
PMC: 6133280.
DOI: 10.1371/journal.pone.0203007.
Haploid yeast cells undergo a reversible phenotypic switch associated with chromosome II copy number.
Drozdova P, Mironova L, Zhouravleva G
BMC Genet. 2017; 17(Suppl 3):152.
PMID: 28105933
PMC: 5249023.
DOI: 10.1186/s12863-016-0464-4.
Fast Bayesian Inference of Copy Number Variants using Hidden Markov Models with Wavelet Compression.
Wiedenhoeft J, Brugel E, Schliep A
PLoS Comput Biol. 2016; 12(5):e1004871.
PMID: 27177143
PMC: 4866742.
DOI: 10.1371/journal.pcbi.1004871.
aCGH-MAS: analysis of aCGH by means of multiagent system.
De Paz J, Benito R, Bajo J, Rodriguez A, Abaigar M
Biomed Res Int. 2015; 2015:194624.
PMID: 25874203
PMC: 4385609.
DOI: 10.1155/2015/194624.
Copy number variation in the horse genome.
Ghosh S, Qu Z, Das P, Fang E, Juras R, Cothran E
PLoS Genet. 2014; 10(10):e1004712.
PMID: 25340504
PMC: 4207638.
DOI: 10.1371/journal.pgen.1004712.
Genome-wide scan identifies a copy number variable region at 3p21.1 that influences the TLR9 expression levels in IgA nephropathy patients.
Sallustio F, Cox S, Serino G, Curci C, Pesce F, De Palma G
Eur J Hum Genet. 2014; 23(7):940-8.
PMID: 25293716
PMC: 4463498.
DOI: 10.1038/ejhg.2014.208.
Mapping of the chromosomal amplification 1p21-22 in bladder cancer.
Scaravilli M, Asero P, Tammela T, Visakorpi T, Saramaki O
BMC Res Notes. 2014; 7:547.
PMID: 25135188
PMC: 4143550.
DOI: 10.1186/1756-0500-7-547.
Detection of candidate tumor driver genes using a fully integrated Bayesian approach.
Yang J, Wang X, Kim M, Xie Y, Xiao G
Stat Med. 2013; 33(10):1784-800.
PMID: 24347204
PMC: 3981913.
DOI: 10.1002/sim.6066.
Bayesian Frequentist hybrid Model wth Application to the Analysis of Gene Copy Number Changes.
Yuan A, Chen G, Xiong J, He W, Rotimi C
J Appl Stat. 2013; 38(5):987-1005.
PMID: 24014930
PMC: 3762327.
DOI: 10.1080/02664761003692449.
Copynumber: Efficient algorithms for single- and multi-track copy number segmentation.
Nilsen G, Liestol K, Van Loo P, Vollan H, Eide M, Rueda O
BMC Genomics. 2013; 13:591.
PMID: 23442169
PMC: 3582591.
DOI: 10.1186/1471-2164-13-591.
Identification of genes for complex diseases by integrating multiple types of genomic data.
Cao H, Lei S, Deng H, Wang Y
Annu Int Conf IEEE Eng Med Biol Soc. 2013; 2012:5541-4.
PMID: 23367184
PMC: 4164202.
DOI: 10.1109/EMBC.2012.6347249.
Identification of genes for complex diseases using integrated analysis of multiple types of genomic data.
Cao H, Lei S, Deng H, Wang Y
PLoS One. 2012; 7(9):e42755.
PMID: 22957024
PMC: 3434191.
DOI: 10.1371/journal.pone.0042755.
Assessing Population Level Genetic Instability via Moving Average.
McDaniel S, Minnier J, Betensky R, Mohapatra G, Shen Y, Gusella J
Stat Biosci. 2012; 2(2):120-136.
PMID: 22866169
PMC: 3409593.
DOI: 10.1007/s12561-010-9028-8.
Detecting simultaneous changepoints in multiple sequences.
Zhang N, Siegmund D, Ji H, Li J
Biometrika. 2012; 97(3):631-645.
PMID: 22822250
PMC: 3372242.
DOI: 10.1093/biomet/asq025.
Change-point analysis of paired allele-specific copy number variation data.
Lai Y
J Comput Biol. 2012; 19(6):679-93.
PMID: 22697241
PMC: 3375654.
DOI: 10.1089/cmb.2012.0031.