Results 61 to 70 of about 912,053 (206)
BackgroundSingle nucleotide polymorphism (SNP) array has been applied to prenatal diagnosis. This study aimed to assess the clinical significance of SNP array in diagnosing fetal chromosomal anomalies based on our experience.MethodsA total of 8753 ...
Li Wen +4 more
doaj +1 more source
Development and validation of a Pacific Abalone (Haliotis discus hannai) custom 60K SNP array
The Pacific abalone (Haliotis discus hannai) is a commercially important abalone species native to South Korea, which is immensely popular as a seafood delicacy.
Jeong Woen Shin +9 more
doaj +1 more source
Tumor Touch Imprints as Source for Whole Genome Analysis of Neuroblastoma Tumors. [PDF]
INTRODUCTION:Tumor touch imprints (TTIs) are routinely used for the molecular diagnosis of neuroblastomas by interphase fluorescence in-situ hybridization (I-FISH).
Clemens Brunner +7 more
doaj +1 more source
Genome-Wide SNP Detection, Validation, and Development of an 8K SNP Array for Apple [PDF]
As high-throughput genetic marker screening systems are essential for a range of genetics studies and plant breeding applications, the International RosBREED SNP Consortium (IRSC) has utilized the Illumina Infinium® II system to develop a medium- to high-
Larry Wilhelm (110561) +94 more
core +3 more sources
Objectives Our study integrates SNP array and metaphase cytogenetics (MC) to decode clonal architecture in myelodysplastic syndromes (MDS) and related disorders.Methods We retrospectively analyzed chromosomal aberrations in 33 patients diagnosed with MDS
Lili Song, Zhenxiu Guo, Kun Chi
doaj +1 more source
Background Cervical carcinoma develops as a result of multiple genetic alterations. Different studies investigated genomic alterations in cervical cancer mainly by means of metaphase comparative genomic hybridization (mCGH) and microsatellite marker ...
Kenter Gemma G +8 more
doaj +1 more source
Single nucleotide polymorphism (SNP) genotyping arrays are powerful tools to measure the level of genetic polymorphism within a population. The coming of next-generation sequencing technologies led to identifying thousands and millions of SNP loci useful
Davide Bianchi +2 more
doaj +1 more source
. Objective:. Isolated hereditary hypotrichosis is caused by mutations in as many as 11 different genes. The conventional mutation detection strategy consists of sequencing of individual candidate genes separately, a time consuming and costly approach ...
Sirous Zeinali +6 more
doaj +1 more source
Original Ashkenazi SNP array data
Original Ashkenazi SNP array data from Gladstein and Hammer 2018.Genotyped on Illumina Omni Express.
Ariella Gladstein (5684096)
core +1 more source
How Array Design affects SNP Ascertainment Bias
Single nucleotide polymorphisms (SNPs), genotyped with SNP arrays, have become a widely used marker type in population genetic analyses over the last 10 years.
Weigend, Annett +5 more
core +1 more source

