Wei Y, Huang G
Sci Rep. 2020; 10(1):10493.
PMID: 32591545
PMC: 7319969.
DOI: 10.1038/s41598-020-64353-1.
Vincenten J, van Essen H, Lissenberg-Witte B, Bulkmans N, Krijgsman O, Sie D
PLoS One. 2019; 14(10):e0223827.
PMID: 31618260
PMC: 6795528.
DOI: 10.1371/journal.pone.0223827.
Peri S, Izumchenko E, Schubert A, Slifker M, Ruth K, Serebriiskii I
Nat Commun. 2017; 8(1):1772.
PMID: 29176703
PMC: 5701248.
DOI: 10.1038/s41467-017-01877-7.
Wang P, Shan L, Xue L, Zheng B, Ying J, Lu N
Oncotarget. 2016; 8(3):5069-5080.
PMID: 27974698
PMC: 5354893.
DOI: 10.18632/oncotarget.13847.
Schutze D, Krijgsman O, Snijders P, Ylstra B, Weischenfeldt J, Mardin B
Oncotarget. 2016; 7(25):37608-37621.
PMID: 26993771
PMC: 5122336.
DOI: 10.18632/oncotarget.8058.
A Systems Biology Interpretation of Array Comparative Genomic Hybridization (aCGH) Data through Phylogenetics.
Abunimer A, Salazar J, Noursi D, Abu-Asab M
OMICS. 2016; 20(3):169-79.
PMID: 26983023
PMC: 4799695.
DOI: 10.1089/omi.2015.0184.
Preserved genetic diversity in organoids cultured from biopsies of human colorectal cancer metastases.
Weeber F, van de Wetering M, Hoogstraat M, Dijkstra K, Krijgsman O, Kuilman T
Proc Natl Acad Sci U S A. 2015; 112(43):13308-11.
PMID: 26460009
PMC: 4629330.
DOI: 10.1073/pnas.1516689112.
Integrating genetics and epigenetics in breast cancer: biological insights, experimental, computational methods and therapeutic potential.
Cava C, Bertoli G, Castiglioni I
BMC Syst Biol. 2015; 9:62.
PMID: 26391647
PMC: 4578257.
DOI: 10.1186/s12918-015-0211-x.
Characterization of cells from patient-derived fibrovascular membranes in proliferative diabetic retinopathy.
Kim L, Wong L, Amarnani D, Bigger-Allen A, Hu Y, Marko C
Mol Vis. 2015; 21:673-87.
PMID: 26120272
PMC: 4462955.
Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice.
Brenndorfer J, Altmann A, Widner-Andra R, Putz B, Czamara D, Tilch E
PLoS One. 2015; 10(5):e0128465.
PMID: 26011321
PMC: 4444327.
DOI: 10.1371/journal.pone.0128465.
Comparison of sequencing based CNV discovery methods using monozygotic twin quartets.
Legault M, Girard S, Lemieux Perreault L, Rouleau G, Dube M
PLoS One. 2015; 10(3):e0122287.
PMID: 25812131
PMC: 4374778.
DOI: 10.1371/journal.pone.0122287.
Focal chromosomal copy number aberrations identify CMTM8 and GPR177 as new candidate driver genes in osteosarcoma.
Both J, Krijgsman O, Bras J, Schaap G, Baas F, Ylstra B
PLoS One. 2015; 9(12):e115835.
PMID: 25551557
PMC: 4281204.
DOI: 10.1371/journal.pone.0115835.
FocalCall: An R Package for the Annotation of Focal Copy Number Aberrations.
Krijgsman O, Benner C, Meijer G, van de Wiel M, Ylstra B
Cancer Inform. 2014; 13:153-6.
PMID: 25506197
PMC: 4251178.
DOI: 10.4137/CIN.S19519.
DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly.
Scheinin I, Sie D, Bengtsson H, van de Wiel M, Olshen A, van Thuijl H
Genome Res. 2014; 24(12):2022-32.
PMID: 25236618
PMC: 4248318.
DOI: 10.1101/gr.175141.114.
Dissecting the gray zone between follicular lymphoma and marginal zone lymphoma using morphological and genetic features.
Krijgsman O, Gonzalez P, Balague Ponz O, Roemer M, Slot S, Broeks A
Haematologica. 2013; 98(12):1921-9.
PMID: 23850804
PMC: 3856968.
DOI: 10.3324/haematol.2013.085118.
Multiscale integration of -omic, imaging, and clinical data in biomedical informatics.
Phan J, Quo C, Cheng C, Wang M
IEEE Rev Biomed Eng. 2012; 5:74-87.
PMID: 23231990
PMC: 5859561.
DOI: 10.1109/RBME.2012.2212427.
Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion.
Gao J, Liu C, Yao F, Hao N, Zhou J, Zhou Q
Mol Cytogenet. 2012; 5(1):33.
PMID: 22794168
PMC: 3488553.
DOI: 10.1186/1755-8166-5-33.
Hybridization and amplification rate correction for affymetrix SNP arrays.
Wang Q, Peng P, Qian M, Wan L, Deng M
BMC Med Genomics. 2012; 5:24.
PMID: 22691279
PMC: 3428662.
DOI: 10.1186/1755-8794-5-24.
Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses.
van Wieringen W, Unger K, Leday G, Krijgsman O, de Menezes R, Ylstra B
BMC Bioinformatics. 2012; 13:80.
PMID: 22559006
PMC: 3475006.
DOI: 10.1186/1471-2105-13-80.
Comparative analysis of algorithms for integration of copy number and expression data.
Louhimo R, Lepikhova T, Monni O, Hautaniemi S
Nat Methods. 2012; 9(4):351-5.
PMID: 22327835
DOI: 10.1038/nmeth.1893.