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INFINIUM Inc methylation epic array reference probes
DNA <t>methylation</t> trend in fasting and postprandial states across BMI classes. Open squares and solid circles, fasting and postprandial state, respectively. Gene name and <t>EPIC</t> array Ow-dmCpG ID are indicated above each graph. N, Ow, and Ob, normal weight, overweight and obese, respectively.
Methylation Epic Array Reference Probes, supplied by INFINIUM Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/methylation+array/epic+dna+methylation+array/pmc08138173-235-54-53
Average 90 stars, based on 1 article reviews
methylation epic array reference probes - by Bioz Stars, 2026-09
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1) Product Images from "Distinct Associations of BMI and Fatty Acids With DNA Methylation in Fasting and Postprandial States in Men"

Article Title: Distinct Associations of BMI and Fatty Acids With DNA Methylation in Fasting and Postprandial States in Men

Journal: Frontiers in Genetics

doi: 10.3389/fgene.2021.665769

DNA methylation trend in fasting and postprandial states across BMI classes. Open squares and solid circles, fasting and postprandial state, respectively. Gene name and EPIC array Ow-dmCpG ID are indicated above each graph. N, Ow, and Ob, normal weight, overweight and obese, respectively.
Figure Legend Snippet: DNA methylation trend in fasting and postprandial states across BMI classes. Open squares and solid circles, fasting and postprandial state, respectively. Gene name and EPIC array Ow-dmCpG ID are indicated above each graph. N, Ow, and Ob, normal weight, overweight and obese, respectively.

Techniques Used: DNA Methylation Assay

Related Articles

other:

Article Title: Epigenome-wide DNA methylation profiling in septic and non-septic patients with similar infections: potential use as sepsis biomarkers
Article Snippet: A discovery cohort of 32 patients was analyzed using Infinium Methylation Array EPIC v2.0 assays.

Article Title: Potentially causal associations between placental DNA methylation and schizophrenia and other neuropsychiatric disorders
Article Snippet: In particular, the fetal brain database was calculated in a limited number of fetal brain samples, in SNP-CpG windows ten times smaller than the ones we used (0.05 Mb vs 0.5 Mb), and DNAm was measured with the Infinium HumanMethylation 450 K array (with approximately half the probes in the Infinium HumanMethylation EPIC array used in the present study), therefore resulting in half a million cis -mQTLs compared to the more than 9 million mQTLs that were included in the SMR analysis in our case.

Article Title: Epigenetic aging differentially impacts breast cancer risk by self-reported race
Article Snippet: In addition, we applied the latest epigenome wide technology (Infinium MethylationEPIC array), and chose multiple measurements of epigenetic aging acceleration, including universal and intrinsic measures.

Methylation:

Article Title: FASN Gene Methylation is Associated with Fatty Acid Synthase Expression and Clinical-genomic Features of Prostate Cancer
Article Snippet: To analyze tumor FASN immunostaining, we utilized three primary tumor cohorts: The first was a previously described radical prostatectomy cohort from 1995 to 2010 of 177 self-identified BL and 194 self-identified White (WH) men, matched by Grade Group from Johns Hopkins (JHU cohort; refs. ). .. We recently published Infinium EPIC methylation profiling data on a subset of this cohort ( ) as described below, and samples were also arrayed on tissue microarray (TMA) for immunostaining studies as described previously ( ). ..

Article Title: Use of Peripheral Intravenous Access in Patients Undergoing Chemotherapy for Testicular Cancer
Article Snippet: Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 3 Laboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, Bethesda, MD Divisions of Human Biology and Clinical Research, Fred Hutchinson Cancer Center, Seattle, WA Department of Urology, Johns Hopkins School of Medicine, Baltimore, MD Department of Oncology, Johns Hopkins School of Medicine, Baltimore, MD

Article Title: Structural variants involving MLLT10 fusion are associated with adverse outcomes in pediatric acute myeloid leukemia
Article Snippet: .. To further determine whether patients with MLLT10 fusions had distinct epigenetic profiles, we performed differential methylation analyses on samples from normal BM and from patients with MLLT10 -rearranged, KMT2A -rearranged, and NUP98 :: NSD1 -fused AML, on the Infinium HumanMethylation EPIC array. ..

Microarray:

Article Title: FASN Gene Methylation is Associated with Fatty Acid Synthase Expression and Clinical-genomic Features of Prostate Cancer
Article Snippet: To analyze tumor FASN immunostaining, we utilized three primary tumor cohorts: The first was a previously described radical prostatectomy cohort from 1995 to 2010 of 177 self-identified BL and 194 self-identified White (WH) men, matched by Grade Group from Johns Hopkins (JHU cohort; refs. ). .. We recently published Infinium EPIC methylation profiling data on a subset of this cohort ( ) as described below, and samples were also arrayed on tissue microarray (TMA) for immunostaining studies as described previously ( ). ..

Article Title: Use of Peripheral Intravenous Access in Patients Undergoing Chemotherapy for Testicular Cancer
Article Snippet: Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 3 Laboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, Bethesda, MD Divisions of Human Biology and Clinical Research, Fred Hutchinson Cancer Center, Seattle, WA Department of Urology, Johns Hopkins School of Medicine, Baltimore, MD Department of Oncology, Johns Hopkins School of Medicine, Baltimore, MD

Immunostaining:

Article Title: FASN Gene Methylation is Associated with Fatty Acid Synthase Expression and Clinical-genomic Features of Prostate Cancer
Article Snippet: To analyze tumor FASN immunostaining, we utilized three primary tumor cohorts: The first was a previously described radical prostatectomy cohort from 1995 to 2010 of 177 self-identified BL and 194 self-identified White (WH) men, matched by Grade Group from Johns Hopkins (JHU cohort; refs. ). .. We recently published Infinium EPIC methylation profiling data on a subset of this cohort ( ) as described below, and samples were also arrayed on tissue microarray (TMA) for immunostaining studies as described previously ( ). ..

Article Title: Use of Peripheral Intravenous Access in Patients Undergoing Chemotherapy for Testicular Cancer
Article Snippet: Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 3 Laboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, Bethesda, MD Divisions of Human Biology and Clinical Research, Fred Hutchinson Cancer Center, Seattle, WA Department of Urology, Johns Hopkins School of Medicine, Baltimore, MD Department of Oncology, Johns Hopkins School of Medicine, Baltimore, MD



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Image Search Results


( A ) Epigenome-wide association study of dpi in PBMCs based on the entire methylation array. The volcano plots display the −log 10 ( P values) and the directionality of association between CpG sites and infection stages (A, EC, and LC) compared with B: A versus B (left panel), EC versus B (center panel), and LC versus B (right panel). Each dot represents a specific DNAme site. Shown are significantly associated CpG sites ( q < 0.05) with hypomethylation (blue), hypermethylation (red), and nonsignificant (gray). The horizontal axis represents the mean methylation change (i.e., the difference between group means), and the vertical axis represents −log 10 ( P values). ( B ) Changes in EA during each infection stage (A, EC, and LC) relative to B. Biological age analysis was performed based on subsets of clock CpGs. EA at the 3 infection time points was compared with B using mixed-effects linear regression modeling of longitudinal EA changes in PBMCs based on 10 epigenetic clocks. The results are shown separately for young (right) and old (left) RMs. Epigenetic age changes in young (blue) and old (red) RMs are shown. Saturated colors indicate statistically significant changes ( P < 0.05); pale colors indicate nonsignificant changes ( P > 0.05). A statistically significant increase in EA was observed only in young RMs. B–H, Benjamini–Hochberg correction; DMP, differentially methylated positions; dpi, days after infection; RMs, rhesus macaques; B, baseline; A, acute; EC, early chronic; LC, late chronic; EA, epigenetic age.

Journal: The Journal of Clinical Investigation

Article Title: Pathogenic SIV infection is associated with acceleration of epigenetic age in rhesus macaques

doi: 10.1172/JCI189574

Figure Lengend Snippet: ( A ) Epigenome-wide association study of dpi in PBMCs based on the entire methylation array. The volcano plots display the −log 10 ( P values) and the directionality of association between CpG sites and infection stages (A, EC, and LC) compared with B: A versus B (left panel), EC versus B (center panel), and LC versus B (right panel). Each dot represents a specific DNAme site. Shown are significantly associated CpG sites ( q < 0.05) with hypomethylation (blue), hypermethylation (red), and nonsignificant (gray). The horizontal axis represents the mean methylation change (i.e., the difference between group means), and the vertical axis represents −log 10 ( P values). ( B ) Changes in EA during each infection stage (A, EC, and LC) relative to B. Biological age analysis was performed based on subsets of clock CpGs. EA at the 3 infection time points was compared with B using mixed-effects linear regression modeling of longitudinal EA changes in PBMCs based on 10 epigenetic clocks. The results are shown separately for young (right) and old (left) RMs. Epigenetic age changes in young (blue) and old (red) RMs are shown. Saturated colors indicate statistically significant changes ( P < 0.05); pale colors indicate nonsignificant changes ( P > 0.05). A statistically significant increase in EA was observed only in young RMs. B–H, Benjamini–Hochberg correction; DMP, differentially methylated positions; dpi, days after infection; RMs, rhesus macaques; B, baseline; A, acute; EC, early chronic; LC, late chronic; EA, epigenetic age.

Article Snippet: DNAme profiles were generated using a custom Infinium methylation array (HorvathMammalMethylChip40) representing 37,492 CpG highly conserved sites in the mammals, with the NCBI’s Gene Expression Omnibus (GEO) accession number GPL28271 for microarray design ( ).

Techniques: Methylation, Infection