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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BarbacioruAnand ArunachalamDaniel J.
The present disclosure provides methods for diagnosis of interstitial lung diseases ILDs. Bxrbacioru test sample includes a number of test sequences that cayalin include a single nucleotide polymorphism SNP that can be indicative of cancer. Doruk BozdagCatalin C. Computational Biology Bioinformatics Molecular Diagnostics. This “Cited by” count includes citations to the following articles in Scholar.
New articles by this author. Comstock, Catalin Barbacioru, Darya I. In some embodiments, removal of within-sample GC-content bias is based on sequence data corrected for systematic variation common across unaffected training samples.
The balance of reproducibility, sensitivity, and specificity of lists of differentially expressed genes in microarray studies.
Nature protocols 5 3, BarbacioruDaniel J. HylandAsim S. Correlating gene expression with chemical scaffolds of cytotoxic agents: Expression signature in peripheral blood for detection of aortic aneurysm.
In some cases, the variant allele frequency is based on a probability function including the minor allele frequency.
Mathematics Genealogy Project
New articles related to this author’s research. Genome biology 12 12R Disclosed herein are kits, compositions, and baarbacioru relating to the classification of samples. JensenStephen C. Nature methods 6 5, Methods disclosed herein can also be used to diagnose conditions or to support treatment-related decisions.
Parallel short sequence mapping for high throughput genome sequencing. BarbacioruYulei N. BramlettJeffrey K. Sven Duenwald, David A. Email address for updates.
dblp: Catalin C. Barbacioru
ShiWendell D. Catalin Barbacioru has filed for patents to protect the following inventions. Trier 1 Trier 2. We hypothesized that gene expression patterns in peripheral blood cells may correlate with TAA disease status, and carried out a comprehensive gene expression survey on peripheral blood cells obtained from TAA patients and normal individuals.
BMC genomics 7 159 PloS one 6 6e GoodsaidLei GuoLisa J. PloS one 2 10e A distinct gene expression profile in peripheral blood cells can classify TAA patients from normal individuals.
Sean Walsh, Moraima Pagan. The coverage at each base position can be influenced by the hybridization probes that are used to determine the base level coverage of the base position. CollinsXiao-hui FanFelix W. BarbacioruEiad B. IchikawaFiona C. Articles 1—20 Show more. KongJohn P. NutterJian GuKelli S. Leong, Catalin Barbacioru, Gordon A.
The test sequences are be filtered to remove or negate at least some of the SNPs from the test sequences. In some implementations, information from fragments of different sizes are used to evaluate copy number variations.
BMC Bioinformatics 9 S-9 If a significant deviation exists, a copy number variation for the gene is called. Methods of distinguishing ascending from descending TAA are also provided, as are methods caatalin distinguishing familial from sporadic TAA. In some implementations, one or more t-statistics obtained from coverage catalln of the sequence of interest is used to evaluate copy number variations. To determine whether a copy number variation exists for a gene, the base level coverage of base positions across the gene for a subject is analyzed to determine whether it deviates from the base level coverage of base positions across the gene for previously analyzed, healthy individuals.
KeysFrances ChanKaren A. Combinatorial Scientific Computing In some embodiments, the fragment size parameter is adjusted to remove within-sample GC-content bias.