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Affymetrix human gene 1.0 st array

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The Affymetrix Human Gene 1.0 ST Array is a gene expression microarray designed for the comprehensive analysis of the human transcriptome. It contains probes targeting well-annotated genes and supports the measurement of gene expression levels across the entire length of each transcript.

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48 protocols using affymetrix human gene 1.0 st array

1

High-Throughput Profiling of Genomic Alterations in HCC

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In the discovery phase, high-throughput screening was performed using Affymetrix Human Gene 1.0 ST Array (Affymetrix, Santa Clara, CA), Nimblegen 3×720 K CpG Island Plus RefSeq Promoter Array (Roche NimbleGen, Madison, WI) and Affymetrix GeneChip Human Mapping 6.0 array (Affymetrix) to measure mRNA expression, DNA methylation and copy number changes in HCCs and paired non-tumor specimens, respectively. Referring to the corresponding array design database, we confirmed that the Affymetrix Human Gene 1.0 ST Array interrogates all 1,027 inflammation-related genes described by Loza et al. [10 (link)] with 1,108 transcripts; and the Nimblegen 3×720 K CpG Island Plus RefSeq Promoter Array and Affymetrix GeneChip Human Mapping 6.0 array interrogate 38,179 probes covering 1,024 genes and 33,855 probes covering 938 genes, respectively.
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2

Circadian Clock Genes in Pancreatic Adenocarcinoma

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Gene expression information of PADA patients was acquired from the Cancer Genome Atlas (TCGA) database and Gene Expression Omnibus (GEO), including GSE62452 [17 (link)] and GSE28735 [18 (link)]. TCGA contains 172 PADA patients with a follow-up time of more than one month, among including of 171 primary tumors and one metastatic tumor. These samples were divided into the discovery set (n = 120) and validation set (n = 52). GSE62452 contains 69 PADA and adjacent non-tumor samples, among which 65 PADA samples had a follow-up time of more than one month. These samples were snap-frozen and sequenced using Affymetrix Human Gene 1.0 ST Array (GPL6244). GSE28735 contains 45 PAD patients, among which 42 PADA patients had a follow-up time of more than one month. These samples were also snap-frozen and sequenced using Affymetrix Human Gene 1.0 ST Array (GPL6244). Gene expression information was got through Cancer Cell Line Encyclopedia (CCLE) database. IC50 values of pancreatic cancer cell lines was got from Genomics of Drug Sensitivity in Cancer (GDSC). In the present study, gene expression profiling from TCGA was subjected to TPM normalization, and all arrays were subjected to RMA normalized in GSE62452 and GSE28735. A total of 104 circadian clock-associated genes that were retrieved in MSigDB database [19 (link)]. Basic information for gene expression data was shown in the Table 1.
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3

Comprehensive Gene Expression Analysis of Primary Immunodeficiency

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According to the information included in the Gene Expression Omnibus (GEO) database [15 (link)] (https://www.ncbi.nlm.nih.gov/geo/ accessed on 15 February 2022), we downloaded the PI-related GSE33774 and GSE57631 genome-wide expression datasets. The GSE33774 dataset included 8 healthy samples and 7 PI samples. GSE33774 platform is GPL6244 [HuGene-1_0-st] Affymetrix Human Gene 1.0 ST Array [transcript (gene) version]. The GSE57631 dataset comprised 2 healthy samples and 6 PI samples, and the platform is GPL15034 [HuGene-1_0-st] Affymetrix Human Gene 1.0 ST Array [HuGene10stv1_Hs_ENTREZ, Brainarray v14].
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4

Transcriptome Analysis of Colitis in IBD

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Raw expression microarray array (CEL data) from the GSE13367, GSE38713, GSE16879, GSE48958, GSE75214, GSE4183, GSE37283, and GSE31106 datasets were downloaded from Gene Expression Omnibus1 (Barrett et al., 2013 (link)). Probe annotations and platform information were generated by matching with the GPL6244 (HuGene-1_0-st) Affymetrix Human Gene 1.0 ST Array (Affymetrix, Santa Clara, CA, United States).
In this study, we analyzed the patients with colitis exclusively, no other IBD cases included. Here, GSE48958 and GSE75214 are matching with the GPL6244 (HuGene-1_0-st) Affymetrix Human Gene 1.0 ST Array, while GSE13367, GSE38713, GSE16879, GSE37283, and GSE4183 are pairing with the GPL570 (HG-U133_Plus_2) Affymetrix Human Genome U133 Plus 2.0 Array and the GSE31106 is in line with GPL1261 (Mouse430_2) Affymetrix Mouse Genome 430 2.0 Array. Total RNA extracted from mucosal biopsies was used to analyze mRNA expression via Affymetrix arrays, and corresponding grouping information from each sample was subsequently pooled for further correlation analysis. Statistical analysis was performed with the R (version 3.3.2).
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5

Microarray Analysis of Human Neuroblastoma Cell Lines

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The GSE78061 dataset (15 (link)) used in the present study was downloaded from GEO (www.ncbi.nlm.nih.gov/geo/), based on the Affymetrix human gene 1.0 ST array (Thermo Fisher Scientific, Inc., Waltham, MA, USA). Expression data from 25 human NB cell lines and four RPE cell lines were analyzed in the GSE78061 dataset.
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6

Gene Expression Profiling of HCC Samples

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Gene expression profile data GSE64041 which was deposited by Makowska et al (16 (link)), was downloaded from Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) database (17 (link)). The datasets were sequenced on the platform Affymetrix Human Gene 1.0 ST Array (Affymetrix; Thermo Fisher Scientific, Inc., Waltham, MA, USA). A total of 60 biopsy pairs from patients with HCC were obtained, including 60 HCC samples and 60 matched non-tumor liver samples.
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7

Retinoblastoma Transcriptome Analysis

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The study was conducted in accordance with the tenets of the Declaration of Helsinki. GSE24673[13 (link)], GSE97508[14 (link)], and GSE110811 [15 (link)] were retrieved from the GEO database (https://www.ncbi.nlm.nih.gov/geo/), an international public repository of microarray profiles. The platform for GSE24673 was GPL6244 (Affymetrix Human Gene 1.0 ST array; Thermo Fisher Scientific, Waltham, MA), which included 9 retinoblastoma samples and 2 normal control retinas. The platform for GSE97508 was GPL15207 (Affymetrix Human Gene Expression Array; Thermo Fisher Scientific), which included 6 retinoblastoma samples and 3 control retinas. The platform for GSE110811 was GPL16686 (Affymetrix Human Gene 2.0 ST array; Thermo Fisher Scientific), which included 28 retinoblastoma samples and 3 control tissues. The H (hallmark) gene sets, C2 curated gene sets, and C5 ontology gene sets were downloaded from the molecular signatures database (MSigDB, https://www.gsea-msigdb.org/gsea/msigdb/)[16 (link)]. Expression profiles, immune subtypes, stem cell transcriptomes, and stem cell DNA methylation data were downloaded from the Xena Functional Genomics Explorer (https://xena.ucsc.edu/)[17 (link)].
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8

Transcriptome Profiling of Cell Lines

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Approximately 5.0 × 105 cells were seeded in T25 flasks in triplicate, incubated for 24 hours and then washed with PBS and trypsinized. RNA was extracted from the cells using the Qiagen RNeasy Blood and Tissue Kit (Qiagen). Amplified cDNA was generated from 200 ng RNA using the Applause WT-Amp ST system (NuGEN, San Carlos, CA) and analysed using Affymetrix Human Gene 1.0ST array on the Genechip Fluidics Station 450 FS450 (Thermo Fisher Scientific). CEL files were loaded into the R Bioconductor environment using the oligo package [41 (link)], normalized using the Robust Multi-Array Average method with the default settings [42 (link)], and assessed using the Linear Models for Microarray method [43 ].
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9

GSE64234 Gene Expression Profile Analysis

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The GSE64234 gene expression profile dataset deposited by de Oliveira et al (10 (link)) was downloaded from the Gene Expression Omnibus (https://www.ncbi.nlm.nih.gov/geo/) database, which was based on the GPL6244 Affymetrix Human Gene 1.0 ST Array (Thermo Fisher Scientific, Inc., Waltham, MA, USA). Data on 12 HL cell line specimens were available in GSE64234, including 6 treated with non-targeting small interfering (si)RNA (control group) and 6 with NFKB2-targeted siRNA (knockdown group).
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10

Differential Gene Expression Analysis of Cisplatin-Resistant Lung Cancer Cells

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The human GSE21656 microarray dataset (20 (link)) was downloaded from the NCBI Gene Expression Omnibus (GEO) database (www.ncbi.nlm.nih.gov/geo). The available dataset, GSE21656 was based on the GPL6244 platform (Affymetrix Human Gene 1.0 ST Array, Affymetrix; Thermo Fisher Scientific, Inc.). This data includes H460 cells and DDP-resistant H460 cells sample, and each cell has three repeats samples. The online tool, GEO2R (http://www.ncbi.nlm.nih.gov/geo/geo2r) (21 (link)) was used to determine the differentially expressed genes in H460 and DDP-resistant H460 cells. P<0.05 and |log2fold-change|≥1 were set as cut-off standards.
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