The current study included 3,215 RS participants who had
both SNP microarray data and 3D MRI.
Principal components analysis of
SNP microarray data was used to identify ancestry outliers.
Natera uses
a SNP microarray from Ilumina with a proprietary technology called Parental Support ™, which tests all 24 chromosomes and delivers results that are typically > 99 % accurate.
One of the techniques she uses is
SNP microarrays, which enable researchers to screen a genetic sample for many SNPs at once on specially designed DNA «chips».
Not exact matches
As novel applications, such as drug screening,
SNP detection, diagnostics, environmental monitoring, and food protection, are developed, there will be more demand for experienced
microarray technicians in the workplace.
Furthermore, they are undertaking an additional validation measure on several
SNPs via the TaqMan ® assay, a non —
microarray - based genotyping method.
Both firms utilize
microarray genotyping to pinpoint hundreds of thousands of single nucleotide polymorphisms (
SNPs) that indicate phenotypic traits such as eye color, hair color, and freckling as well as geographic ancestry.
Bioinformatics services include data QC, outlier detection and general data management, and data analysis from platforms including Illumina or Affymetrix
microarrays, RNA - Seq,
SNP arrays, Exome - sequencing, ChIP - chips and CHIP - seq.
With all of the
SNP genotypes in hand, researchers could assess gene expression — initially with
microarrays, and later with RNA - seq — and then correlate it with genetic variation.
Laurence Rubin, Identitas CEO and a practicing rheumatologist at St. Michael's Hospital in Toronto, says that his company is now shifting gears from demonstrating the utility of
SNP - based
microarrays for analyzing forensic samples to into more of an advocacy role, introducing law enforcement agencies to the power of these genomic technologies.
After initially applying the genomic
SNP chromosomal
microarray only in fetuses with ultrasound abnormalities, since July 2012, we routinely performed the
SNP array also in cases without fetal ultrasound anomalies where invasive prenatal diagnosis was indicated.
Most of these compare gene expression data (
microarray or RNA - seq) to high - density
SNP array genotypes.
Experienced in developing pipelines and subsequent analysis / interpretation of high - throughput array data (
microarrays,
SNPs and CNVs), NGS data (RNA - Seq, miRNA - Seq and ChIP -...