نتایج جستجو برای: oligonucleotide array sequence analysis

تعداد نتایج: 3216786  

Journal: :Genome research 1998
T R Gingeras G Ghandour E Wang A Berno P M Small F Drobniewski D Alland E Desmond M Holodniy J Drenkow

High-density oligonucleotide arrays can be used to rapidly examine large amounts of DNA sequence in a high throughput manner. An array designed to determine the specific nucleotide sequence of 705 bp of the rpoB gene of Mycobacterium tuberculosis accurately detected rifampin resistance associated with mutations of 44 clinical isolates of M. tuberculosis. The nucleotide sequence diversity in 121...

Journal: :Science 2000
T A Taton C A Mirkin R L Letsinger

A method for analyzing combinatorial DNA arrays using oligonucleotide-modified gold nanoparticle probes and a conventional flatbed scanner is described here. Labeling oligonucleotide targets with nanoparticle rather than fluorophore probes substantially alters the melting profiles of the targets from an array substrate. This difference permits the discrimination of an oligonucleotide sequence f...

Journal: :PLoS ONE 2008
Michael A. Cook Chi-Kin Chan Paul Jorgensen Troy Ketela Daniel So Mike Tyers Chi-Yip Ho

BACKGROUND Molecular barcode arrays provide a powerful means to analyze cellular phenotypes in parallel through detection of short (20-60 base) unique sequence tags, or "barcodes", associated with each strain or clone in a collection. However, costs of current methods for microarray construction, whether by in situ oligonucleotide synthesis or ex situ coupling of modified oligonucleotides to th...

2008
Ricardo Carnicer Mario A. Guzman Sergio Acin Joaquin C. Surra Maria A. Navarro Jose M. Arbones-Mainar Carmen Arnal Rosa Morales Jesus Osada

1. Abstract 2. Introduction 3. Material and Methods 3.1. Animals 3.2. PCR Genotyping 3.3. Plasma determinations 3.4. Blood pressure 3.5. Histological analysis 3.6. RNA isolation, Affymetrix oligonucleotide array hybridization, and data analysis 3.7. Statistical analysis 4. Results 4.1. Plasma biochemistry 4.2. Arterial blood pressure 4.3. Plasma NO levels 4.4. Histological analyses of aorta 4.5...

Journal: :Croatian medical journal 2003
Matthew N Gabriel Cassandra D Calloway Rebecca L Reynolds Dragan Primorac

AIM A rapid analysis of mitochondrial DNA (mtDNA) sequences with an array of immobilized sequence-specific oligonucleotide (SSO) probes was tested on 18 skeletal elements recovered from mass graves in Croatia, which could not be genotyped with common forensic nuclear DNA systems (PM+DQA1 and short tandem repeat analysis). METHODS We used duplex polymerase chain reaction (PCR) amplification of...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تحصیلات تکمیلی علوم پایه زنجان - دانشکده شیمی 1391

in this thesis a calibration transfer method is used to achieve bilinearity for augmented first order kinetic data. first, the proposed method is investigated using simulated data and next the concept is applied to experimental data. the experimental data consists of spectroscopic monitoring of the first order degradation reaction of carbaryl. this component is used for control of pests in frui...

Journal: :Colloids and surfaces. B, Biointerfaces 2005
P F Xiao Z F Wang H S Guo N Y He Z H Lu

In this paper, a simple, reliable and flexible method, which integrated in situ synthesis with the spotting technique, was reported to fabricate oligonucleotide array. Different oligonucleotide sequences are synthesized on their relative code glass slides through combinational chemistry, thus the slides are broken into smaller pieces, in which the same code pieces have the same probe sequences....

2007
Pan Du Warren A. Kibbe Simon M. Lin Robert H. Lurie

Gene Identifier v.s. Oligonucleotide Identifier Oligonucleotides (often simply referred to as oligos or oligomers), which are typically between 25 to 75 bases long, have been extensively used by DNA microarray manufacturers to detect the expression of different genes. An oligonucleotide sequence that is located on a specific bead or position on a microarray is usually referred to as the probe s...

Journal: :Journal of clinical microbiology 2012
Stephan Olschläger Stephan Günther

To facilitate sequence-specific detection of DNA amplified in a diagnostic reverse transcription (RT)-PCR for Lassa virus, we developed an array featuring 47 oligonucleotide probes for post-PCR hybridization of the amplicons. The array procedure may be performed with low-tech equipment and does not take longer than agarose gel detection.

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