methylation analysis using Search Results


methylation analysis for multiple id-associated dmrs using  (Pyrosequencing Inc)
90
Pyrosequencing Inc methylation analysis for multiple id-associated dmrs using
Heatmap of <t>array-based</t> <t>methylation</t> analysis using analysis method 1 . The heatmap indicates 56 aberrant <t>DMRs</t> out of 78 examined DMRs. Each row represents a DMR; each column represents a patient. Germline DMRs are shown on a gray background, secondary DMRs on a light green background, and unclassifiable DMRs on a white background. Methylation disturbances of DMRs are classified into seven categories based on the degree. B, Beckwith-Wiedemann syndrome; P, pseudohypoparathyroidism type 1B; O, overgrowth; S, Silver-Russell syndrome; TS, Temple syndrome; TN, transient neonatal diabetes mellitus; W, Prader-Willi syndrome; SG, small for gestational age; N, neurodevelopmental delay and/or intellectual developmental disorder; A, assisted reproductive technology; T, monozygotic monochorionic diamniotic twins; V, variants of uncertain significance; L, likely pathogenic; DMR, differential methylated region; Chr, chromosome; MML, median methylation level of CpG sites in the DMR; SD, standard deviation; mean, mean MML of 16 healthy controls
Methylation Analysis For Multiple Id Associated Dmrs Using, supplied by Pyrosequencing 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/result/methylation analysis for multiple id-associated dmrs using/product/Pyrosequencing Inc
Average 90 stars, based on 1 article reviews
methylation analysis for multiple id-associated dmrs using - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
high-performance and high-accuracy tool for methylation analysis using precise whole-genome sequencing  (Oxford Nanopore)
90
Oxford Nanopore high-performance and high-accuracy tool for methylation analysis using precise whole-genome sequencing
Heatmap of <t>array-based</t> <t>methylation</t> analysis using analysis method 1 . The heatmap indicates 56 aberrant <t>DMRs</t> out of 78 examined DMRs. Each row represents a DMR; each column represents a patient. Germline DMRs are shown on a gray background, secondary DMRs on a light green background, and unclassifiable DMRs on a white background. Methylation disturbances of DMRs are classified into seven categories based on the degree. B, Beckwith-Wiedemann syndrome; P, pseudohypoparathyroidism type 1B; O, overgrowth; S, Silver-Russell syndrome; TS, Temple syndrome; TN, transient neonatal diabetes mellitus; W, Prader-Willi syndrome; SG, small for gestational age; N, neurodevelopmental delay and/or intellectual developmental disorder; A, assisted reproductive technology; T, monozygotic monochorionic diamniotic twins; V, variants of uncertain significance; L, likely pathogenic; DMR, differential methylated region; Chr, chromosome; MML, median methylation level of CpG sites in the DMR; SD, standard deviation; mean, mean MML of 16 healthy controls
High Performance And High Accuracy Tool For Methylation Analysis Using Precise Whole Genome Sequencing, supplied by Oxford Nanopore, 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/result/high-performance and high-accuracy tool for methylation analysis using precise whole-genome sequencing/product/Oxford Nanopore
Average 90 stars, based on 1 article reviews
high-performance and high-accuracy tool for methylation analysis using precise whole-genome sequencing - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
“training instructions for epityper quantitative methylation analysis using masscleave for massarray”  (Sequenom)
90
Sequenom “training instructions for epityper quantitative methylation analysis using masscleave for massarray”
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
“Training Instructions For Epityper Quantitative Methylation Analysis Using Masscleave For Massarray”, supplied by Sequenom, 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/result/“training instructions for epityper quantitative methylation analysis using masscleave for massarray”/product/Sequenom
Average 90 stars, based on 1 article reviews
“training instructions for epityper quantitative methylation analysis using masscleave for massarray” - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
genome-wide methylation analysis using illumina infiniummethylationepic beadchips  (Illumina Inc)
90
Illumina Inc genome-wide methylation analysis using illumina infiniummethylationepic beadchips
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
Genome Wide Methylation Analysis Using Illumina Infiniummethylationepic Beadchips, supplied by Illumina 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/result/genome-wide methylation analysis using illumina infiniummethylationepic beadchips/product/Illumina Inc
Average 90 stars, based on 1 article reviews
genome-wide methylation analysis using illumina infiniummethylationepic beadchips - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
methylation analysis using ms-mlpa and/or  (Pyrosequencing Inc)
90
Pyrosequencing Inc methylation analysis using ms-mlpa and/or
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
Methylation Analysis Using Ms Mlpa And/Or, supplied by Pyrosequencing 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/result/methylation analysis using ms-mlpa and/or/product/Pyrosequencing Inc
Average 90 stars, based on 1 article reviews
methylation analysis using ms-mlpa and/or - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
hplc analysis chromatogram of biotransformation of 1-methyl-3.4-dihydroisoquinoline 7a using daicel chiralpak®ic column  (Daicel Corporation)
90
Daicel Corporation hplc analysis chromatogram of biotransformation of 1-methyl-3.4-dihydroisoquinoline 7a using daicel chiralpak®ic column
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
Hplc Analysis Chromatogram Of Biotransformation Of 1 Methyl 3.4 Dihydroisoquinoline 7a Using Daicel Chiralpak®Ic Column, supplied by Daicel Corporation, 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/result/hplc analysis chromatogram of biotransformation of 1-methyl-3.4-dihydroisoquinoline 7a using daicel chiralpak®ic column/product/Daicel Corporation
Average 90 stars, based on 1 article reviews
hplc analysis chromatogram of biotransformation of 1-methyl-3.4-dihydroisoquinoline 7a using daicel chiralpak®ic column - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
methyl laurate with a purity of > 98%, which was used as the internal standard for the gas chromatographic analysis  (FUJIFILM)
90
FUJIFILM methyl laurate with a purity of > 98%, which was used as the internal standard for the gas chromatographic analysis
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
Methyl Laurate With A Purity Of > 98%, Which Was Used As The Internal Standard For The Gas Chromatographic Analysis, supplied by FUJIFILM, 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/result/methyl laurate with a purity of > 98%, which was used as the internal standard for the gas chromatographic analysis/product/FUJIFILM
Average 90 stars, based on 1 article reviews
methyl laurate with a purity of > 98%, which was used as the internal standard for the gas chromatographic analysis - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
hplc analysis of methyl ester of 3n using daicel chiralpak ia column  (Daicel Corporation)
90
Daicel Corporation hplc analysis of methyl ester of 3n using daicel chiralpak ia column
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
Hplc Analysis Of Methyl Ester Of 3n Using Daicel Chiralpak Ia Column, supplied by Daicel Corporation, 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/result/hplc analysis of methyl ester of 3n using daicel chiralpak ia column/product/Daicel Corporation
Average 90 stars, based on 1 article reviews
hplc analysis of methyl ester of 3n using daicel chiralpak ia column - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
amplicon based deep sequencing methylation analysis using  (Illumina Inc)
90
Illumina Inc amplicon based deep sequencing methylation analysis using
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
Amplicon Based Deep Sequencing Methylation Analysis Using, supplied by Illumina 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/result/amplicon based deep sequencing methylation analysis using/product/Illumina Inc
Average 90 stars, based on 1 article reviews
amplicon based deep sequencing methylation analysis using - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
hplc analysis of methyl ester of 3a using daicel chiralpak ia column  (Daicel Corporation)
90
Daicel Corporation hplc analysis of methyl ester of 3a using daicel chiralpak ia column
A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. <t>MassARRAY</t> results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).
Hplc Analysis Of Methyl Ester Of 3a Using Daicel Chiralpak Ia Column, supplied by Daicel Corporation, 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/result/hplc analysis of methyl ester of 3a using daicel chiralpak ia column/product/Daicel Corporation
Average 90 stars, based on 1 article reviews
hplc analysis of methyl ester of 3a using daicel chiralpak ia column - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

Image Search Results


Heatmap of array-based methylation analysis using analysis method 1 . The heatmap indicates 56 aberrant DMRs out of 78 examined DMRs. Each row represents a DMR; each column represents a patient. Germline DMRs are shown on a gray background, secondary DMRs on a light green background, and unclassifiable DMRs on a white background. Methylation disturbances of DMRs are classified into seven categories based on the degree. B, Beckwith-Wiedemann syndrome; P, pseudohypoparathyroidism type 1B; O, overgrowth; S, Silver-Russell syndrome; TS, Temple syndrome; TN, transient neonatal diabetes mellitus; W, Prader-Willi syndrome; SG, small for gestational age; N, neurodevelopmental delay and/or intellectual developmental disorder; A, assisted reproductive technology; T, monozygotic monochorionic diamniotic twins; V, variants of uncertain significance; L, likely pathogenic; DMR, differential methylated region; Chr, chromosome; MML, median methylation level of CpG sites in the DMR; SD, standard deviation; mean, mean MML of 16 healthy controls

Journal: Clinical Epigenetics

Article Title: Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance

doi: 10.1186/s13148-024-01744-5

Figure Lengend Snippet: Heatmap of array-based methylation analysis using analysis method 1 . The heatmap indicates 56 aberrant DMRs out of 78 examined DMRs. Each row represents a DMR; each column represents a patient. Germline DMRs are shown on a gray background, secondary DMRs on a light green background, and unclassifiable DMRs on a white background. Methylation disturbances of DMRs are classified into seven categories based on the degree. B, Beckwith-Wiedemann syndrome; P, pseudohypoparathyroidism type 1B; O, overgrowth; S, Silver-Russell syndrome; TS, Temple syndrome; TN, transient neonatal diabetes mellitus; W, Prader-Willi syndrome; SG, small for gestational age; N, neurodevelopmental delay and/or intellectual developmental disorder; A, assisted reproductive technology; T, monozygotic monochorionic diamniotic twins; V, variants of uncertain significance; L, likely pathogenic; DMR, differential methylated region; Chr, chromosome; MML, median methylation level of CpG sites in the DMR; SD, standard deviation; mean, mean MML of 16 healthy controls

Article Snippet: Consequently, we identified MLID in 29 patients with epimutation confirmed by methylation analysis for multiple ID-associated DMRs using pyrosequencing and/or methylation-specific multiple ligation-dependent probe amplification.

Techniques: Methylation, Standard Deviation

A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. MassARRAY results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).

Journal: Oncotarget

Article Title: DNA methylation promotes paired box 2 expression via myeloid zinc finger 1 in endometrial cancer

doi: 10.18632/oncotarget.12626

Figure Lengend Snippet: A. Bisulfite sequencing results showed fragment B1 (-764 to -447 bp) of the PAX2 promoter was hypermethylated in endometrial cancer cell lines and tissues: rows represent clones (10 for each sample), columns represent CpG sites. Black squares represent methylated CpGs, and white squares represent unmethylated CpGs. EEC: endometrial epithelial cell. EnCa: endometrial cancer. N: normal. B. MassARRAY results indicate that PAX2 was hypermethylated in endometrial cancer tissues compared with normal endometrial tissues. M1 is an amplicon of a 280-bp fragment from -723 bp to -443 bp; M2 is an amplicon of a 379-bp fragment from -468 bp to -89 bp. Hypermethylated CpG sites were centralized in the 5’ of M1 (CpG 1 to 7).

Article Snippet: The PCR annealing Tm was 56°C, and sample preparation was performed according to “Training Instructions for EpiTYPER Quantitative Methylation Analysis Using MassCLEAVE for MassARRAY” (Sequenom).

Techniques: Methylation Sequencing, Clone Assay, Methylation, Amplification