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.
|Published (Last):||15 October 2017|
|PDF File Size:||15.92 Mb|
|ePub File Size:||6.43 Mb|
|Price:||Free* [*Free Regsitration Required]|
For each gene, coverage at each base position across the gene is determined. BarbacioruEiad B. WangRoger D.
Catalin Barbacioru – The Mathematics Genealogy Project
Comstock, Catalin Barbacioru, Darya I. CatalinnCatalin C. JensenStephen C. HarrisRoger PerkinsFederico M. CowdenEiad B. Leong, Catalin Barbacioru, Gordon A. Jones, Gengxin Chen, Dimitri Skvortsov. Molecular bioSystems 7 12, GoodsaidLei GuoLisa J.
PloS one 6 6e BarbacioruSowmi UtiramerurPenn P.
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. KahwashJoel H.
Sven Duenwald, David A. 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. If a significant deviation exists, a copy number variation for the gene is called.
The present disclosure provides methods for differential diagnosis of idiopathic pulmonary fibrosis from other ILDs. Combinatorial Scientific Computing Gene copy number variations are identified for genes in a targeted gene panel. New articles related to this author’s research. BarbacioruAnand ArunachalamDaniel J. Each test sample includes a number of test sequences that may include a single nucleotide polymorphism SNP that can be indicative of cancer.
Cross-contamination of the test sample is determined if the determined contamination level is above a threshold and statistically significant.
Genome biology 12 12R WhitleyJoel P.
BMC Bioinformatics 9 S-9 The base level coverage for each base position is normalized to account for the characteristics of the hybridization probes. Doruk BozdagCatalin C. To determine whether a copy number variation exists for a gene, the base level coverage of base positions across catlain 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.
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.
Cross-contamination of a test catalon used to determine cancer is identified using gene sequencing data. Negating the test sequences allows more test sequences to be simultaneously analyzed to determine cross-contamination.
CanalesYongming A. CowdenJoel H.
Mathematics Genealogy Project
In some embodiments, methods are provided for determining copy number variation of fetuses using maternal samples comprising maternal and fetal cell free DNA. New citations to this author. Computational Biology Bioinformatics Molecular Diagnostics. In some embodiments, the fragment size parameter is adjusted to remove within-sample GC-content bias.