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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In some embodiments, methods are provided for determining copy number variation of fetuses using maternal samples comprising maternal and fetal cell free DNA. Cancer research 64 12, Catalin Barbacioru has filed for patents to protect the following inventions.

Onur Sakarya, Catalin Barbacioru. Additionally, the methods provide for the determination of a confidence value for a copy number assigned to a sample based on attributes of the sample data. Negating the test sequences allows more test sequences to be simultaneously analyzed to determine cross-contamination. Bmc Bioinformatics 7 1, 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.

Membrane transporters and channels: New citations to this author.

My profile My library Metrics Alerts. BarbacioruEiad B. The test sequences are be filtered to remove or negate at least some of the SNPs from the test sequences. CowdenJoel H. BMC Bioinformatics 9 S-9 BodeauRobert C. GoodsaidLei GuoLisa J. Nature genetics 40 3, PLoS Computational Biology 8 4 CowdenCatalin C. The following articles are merged in Scholar. 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.


Nature protocols 5 3, Methods for the determination of a copy number of a target genomic sequence; either a target gene or genomic sequence of interest, in a biological sample are described.

PloS one 6 6e Methods disclosed herein can also be used to diagnose conditions or to support treatment-related decisions. Jones, Gengxin Chen, Dimitri Skvortsov.

Mathematics Genealogy Project

Pharmacokinetic Mapping of Breast Tumors: Expression signature in peripheral blood for detection of aortic aneurysm. PoulterRaymond R. SunDavid N. KahwashCatalin C. In some embodiments, removal of within-sample GC-content bias is based on sequence data corrected for systematic variation common across unaffected training samples. badbacioru

Catalin Barbacioru – The Mathematics Genealogy Project

For each gene, coverage at each base position across the gene is determined. Nature biotechnology 24 9, NutterJian GuKelli S. This “Cited by” count includes barbaciorru to the following articles in Scholar. BarabcioruJohn P. Effect of various normalization methods on Applied Biosystems expression array system data.


The pharmacogenomics journal 5 2, 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.

Each test sample includes a number of test sequences that may include a single nucleotide polymorphism SNP that can cagalin indicative of cancer. PloS one 2 10e In some embodiments, methods are provided for determining copy number variation CNV of fetuses using maternal samples comprising maternal and fetal cell free DNA. Disclosed are methods for determining copy number variation CNV known or suspected to be associated with a variety of medical conditions.

The present disclosure provides methods for differential diagnosis of idiopathic pulmonary fibrosis from other ILDs.

Cross-contamination is determined by modeling the variant allele frequency for the test sequences as a function of minor allele barbaciooru, contamination level, and background noise. New articles by this author. Get my own profile Cited by View all All Since Citations h-index 25 19 iindex 27 Their combined citations are counted only for the first article.

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