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Infinium human omni express exome 8 v1.2 chip

Manufactured by Illumina

The Infinium Human Omni Express Exome-8 v1.2 chip is a high-density genotyping microarray designed by Illumina. It is capable of interrogating over 4 million genetic markers across the human genome, including coding and non-coding regions. The chip is optimized for whole-exome sequencing analysis.

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2 protocols using infinium human omni express exome 8 v1.2 chip

1

Exon-level DRG Analysis of CA8

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CA8 exon-level DRG analyses were run essentially as described elsewhere [35 (link)]. Briefly, bilateral L4 and L5 DRG were collected from a total of 214 brain-dead human subjects following asystole after consent of family members and snap-frozen. Genomic DNA was isolated and genotyped using Illumina’s Infinium Human Omni Express Exome-8 v1.2 chip (≈ 1M probes) and analyzed using Illumina Genome Studio 2011.1, as described. RNA was isolated from the same DRG samples frozen in TRIzol reagent (Qiagen, Austin, TX). Total RNA was analyzed using Affymetrix Human Transcriptome Array 2.0 (≈ 70K gene-level probes, ≈ 900K isoform-level probes). All statistical tests were performed with age, gender, sample’s average expression and the first two eigenvectors (from principal components analysis to capture racial/ethnic differences) per chromosome as covariates. eQTL discovery was performed on CA8 utilizing 20 exon-level probes that recognize 4 unique CA8 gene transcripts with an expression intensity level above 3. Dataset for eQTL results can be found at GSE78150 (Geo Accession; NCBI).
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2

Genomic DNA Isolation and Genotyping from DRG Tissue

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Genomic DNA was isolated from frozen and homogenized DRG tissue using a QIAamp DNA Mini kit (Qiagen, Austin, TX, US). The genotyping was done on Illumina’s Infinium Human Omni Express Exome-8 v1.2 chip (~1M probes). Arrays were scanned using Illumina iScan, and data analyzed using Illumina Genome Studio 2011.1 with Genotyping module 1.9.4 (Illumina Inc., San Diego, CA, USA). Imputation of the data followed: pre-phasing was performed with SHAPEIT version v2.r790 (O’Connell et al., 2014 (link)) with phase 3 data of the 1,000 genomes project, followed by imputation with impute2 version 2.3.2 (Howie et al., 2012 (link)), again with the 1,000 genomes project phase 3 data.
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