Catalin Barbacioru’s 2 research works with 18 citations and reads, including: aan Rare trisomy SuppMaterial Pertile Catalin Barbacioru has. Catalin Barbacioru’s 81 research works with citations and reads, including: ngS1. Catalin Barbacioru has expertise in Biology and Medicine. USPTO patent applications submitted by and patents granted to Catalin Barbacioru.
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Onur Sakarya, Catalin Barbacioru. Computational Biology Bioinformatics Molecular Diagnostics.
Cross-contamination of the test sample is determined if the determined contamination level is above a threshold and statistically significant. CanalesYongming A. Get my own profile Cited by View all All Since Citations h-index 25 19 iindex 27 The balance of reproducibility, sensitivity, and specificity of lists of differentially expressed barbaciorh in microarray studies.
BMC Bioinformatics 9 S-9 Disclosed herein are kits, compositions, and methods relating to the classification of samples. Methods for the determination of a copy number of a target genomic sequence; either a target gene or genomic sequence of catalkn, in a biological sample are described.
WhitleyJoel P. ShiWendell D.
Molecular bioSystems 7 12, PloS one 2 10e The system can’t perform the operation now. The genes provided by the present teachings define a set of diagnostic markers, thus providing a blood-based gene expression test to facilitate early detection of TAA disease.
Negating the test sequences allows more test sequences to be simultaneously analyzed to determine cross-contamination. The following articles are merged in Scholar. Genome biology 12 12R In some embodiments, methods are provided for determining CNVs known or suspected to be associated with a variety of medical conditions.
IchikawaFiona C. In some embodiments, methods are provided for determining copy number variation of fetuses using maternal samples comprising maternal and fetal cell free DNA. Various methods utilize a model drawn from a probability density function PDF for the assignment of a copy number of a target genomic sequence in a biological sample. In some embodiments, methods are provided for determining copy number variation CNV of fetuses using maternal samples comprising maternal and fetal cell free DNA.
Bmc Bioinformatics 7 1, PLoS Computational Biology 8 4 This “Cited by” count includes citations to the following articles in Scholar. In some embodiments, removal of within-sample GC-content bias is based on sequence data corrected for systematic variation common across unaffected training samples.
In some implementations, information from fragments of different sizes are used to evaluate copy number catakin.
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Expression signature in peripheral blood for detection of aortic aneurysm. Each test sample includes a number of test sequences that may include a single nucleotide polymorphism SNP that can be indicative of cancer. Cancer research 64 12, WangCatalin C. BarbacioruDaniel J.
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Effect of various normalization methods on Applied Biosystems expression array system data. Trier 1 Trier 2. HarrisRoger PerkinsFederico M.
In some cases, the variant allele frequency is based on a probability function including the minor allele frequency.