dna methylation by pyrosequencing assay Search Results


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Pyrosequencing Inc pcr-pyrosequencing
Table 1. Cervical <t> DNA methylation </t> of the prostaglandin E receptor 2 ( PTGER2) and long interspersed nuclear element-1 (LINE 1-HS) ELEMENT birth cohort, Mexico City
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Zymo Research methylation pyrosequencing analyses
Table 1. Cervical <t> DNA methylation </t> of the prostaglandin E receptor 2 ( PTGER2) and long interspersed nuclear element-1 (LINE 1-HS) ELEMENT birth cohort, Mexico City
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Pyrosequencing Inc methylation analysis
Table 1. Cervical <t> DNA methylation </t> of the prostaglandin E receptor 2 ( PTGER2) and long interspersed nuclear element-1 (LINE 1-HS) ELEMENT birth cohort, Mexico City
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Table 1. Cervical <t> DNA methylation </t> of the prostaglandin E receptor 2 ( PTGER2) and long interspersed nuclear element-1 (LINE 1-HS) ELEMENT birth cohort, Mexico City
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Pyrosequencing Inc methylation enrichment pyrosequencing
Diagrammatic representation of primer alignment on sodium bisulphite-treated p16 promoter sequence. Cytosines in squares indicate the nucleotides interrogated by pyrosequencing in PMA and MEP assays (i.e. CpG dinucleotides). The T nucleotide in a square indicates the bisulphite control of these assays (site of non-CpG cytosine). MEP, <t>methylation</t> enrichment PCR primers; PMA, pyrosequencing methylation assay primers; PSEQ, pyrosequencing primer; MSP, methylation-specific PCR primers (primers specific for unmethylated target DNA contain T in squares; primers specific for methylated DNA target contain C in squares).
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Image Search Results


Table 1. Cervical  DNA methylation  of the prostaglandin E receptor 2 ( PTGER2) and long interspersed nuclear element-1 (LINE 1-HS) ELEMENT birth cohort, Mexico City

Journal: Epigenetics

Article Title: Association between length of gestation and cervical DNA methylation of PTGER2 and LINE 1-HS

doi: 10.4161/epi.29170

Figure Lengend Snippet: Table 1. Cervical DNA methylation of the prostaglandin E receptor 2 ( PTGER2) and long interspersed nuclear element-1 (LINE 1-HS) ELEMENT birth cohort, Mexico City

Article Snippet: We performed DNA methylation analyses on bisulfite-treated DNA using a quantitative analysis based on PCR-pyrosequencing.

Techniques: DNA Methylation Assay

Table 2. Associations of maternal characteristics and cervical  DNA methylation,  ELEMENT birth cohort, Mexico City

Journal: Epigenetics

Article Title: Association between length of gestation and cervical DNA methylation of PTGER2 and LINE 1-HS

doi: 10.4161/epi.29170

Figure Lengend Snippet: Table 2. Associations of maternal characteristics and cervical DNA methylation, ELEMENT birth cohort, Mexico City

Article Snippet: We performed DNA methylation analyses on bisulfite-treated DNA using a quantitative analysis based on PCR-pyrosequencing.

Techniques: DNA Methylation Assay

Figure 1. Cervical prostaglandin E receptor 2 (subtype EP2) (PTGER2) DNA methylation and gestational age (days), ELEMENT birth cohort, Mexico City (n = 73).

Journal: Epigenetics

Article Title: Association between length of gestation and cervical DNA methylation of PTGER2 and LINE 1-HS

doi: 10.4161/epi.29170

Figure Lengend Snippet: Figure 1. Cervical prostaglandin E receptor 2 (subtype EP2) (PTGER2) DNA methylation and gestational age (days), ELEMENT birth cohort, Mexico City (n = 73).

Article Snippet: We performed DNA methylation analyses on bisulfite-treated DNA using a quantitative analysis based on PCR-pyrosequencing.

Techniques: DNA Methylation Assay

Figure 2. Cervical long interspersed nuclear element-1 Homo sapiens specific (LINE 1-HS) DNA methylation and gestational age (days), ELEMENT birth cohort, Mexico City (n = 74).

Journal: Epigenetics

Article Title: Association between length of gestation and cervical DNA methylation of PTGER2 and LINE 1-HS

doi: 10.4161/epi.29170

Figure Lengend Snippet: Figure 2. Cervical long interspersed nuclear element-1 Homo sapiens specific (LINE 1-HS) DNA methylation and gestational age (days), ELEMENT birth cohort, Mexico City (n = 74).

Article Snippet: We performed DNA methylation analyses on bisulfite-treated DNA using a quantitative analysis based on PCR-pyrosequencing.

Techniques: DNA Methylation Assay

Figure 3. Gestational Age Differences per interquartile range of cervical DNA methylation of PTGER2 and LINE 1-HS, ELEMENT birth cohort, Mexico City. Model 1: Unadjusted Model 2: Adjusted for maternal age Model 3: Model 2 additionally adjusted for Pap smear inflammation Abbreviations: PTGER2 prostaglandin E receptor 2 (subtype EP2); LINE 1-HS long interspersed nuclear element-1 Homo sapiens-specific. Footnote: n = 69 for PTGER2 models and n = 71 for LINE 1-HS models; error bars indicate 95% confidence intervals.

Journal: Epigenetics

Article Title: Association between length of gestation and cervical DNA methylation of PTGER2 and LINE 1-HS

doi: 10.4161/epi.29170

Figure Lengend Snippet: Figure 3. Gestational Age Differences per interquartile range of cervical DNA methylation of PTGER2 and LINE 1-HS, ELEMENT birth cohort, Mexico City. Model 1: Unadjusted Model 2: Adjusted for maternal age Model 3: Model 2 additionally adjusted for Pap smear inflammation Abbreviations: PTGER2 prostaglandin E receptor 2 (subtype EP2); LINE 1-HS long interspersed nuclear element-1 Homo sapiens-specific. Footnote: n = 69 for PTGER2 models and n = 71 for LINE 1-HS models; error bars indicate 95% confidence intervals.

Article Snippet: We performed DNA methylation analyses on bisulfite-treated DNA using a quantitative analysis based on PCR-pyrosequencing.

Techniques: DNA Methylation Assay

Diagrammatic representation of primer alignment on sodium bisulphite-treated p16 promoter sequence. Cytosines in squares indicate the nucleotides interrogated by pyrosequencing in PMA and MEP assays (i.e. CpG dinucleotides). The T nucleotide in a square indicates the bisulphite control of these assays (site of non-CpG cytosine). MEP, methylation enrichment PCR primers; PMA, pyrosequencing methylation assay primers; PSEQ, pyrosequencing primer; MSP, methylation-specific PCR primers (primers specific for unmethylated target DNA contain T in squares; primers specific for methylated DNA target contain C in squares).

Journal: Nucleic Acids Research

Article Title: Methylation enrichment pyrosequencing: combining the specificity of MSP with validation by pyrosequencing

doi: 10.1093/nar/gkl424

Figure Lengend Snippet: Diagrammatic representation of primer alignment on sodium bisulphite-treated p16 promoter sequence. Cytosines in squares indicate the nucleotides interrogated by pyrosequencing in PMA and MEP assays (i.e. CpG dinucleotides). The T nucleotide in a square indicates the bisulphite control of these assays (site of non-CpG cytosine). MEP, methylation enrichment PCR primers; PMA, pyrosequencing methylation assay primers; PSEQ, pyrosequencing primer; MSP, methylation-specific PCR primers (primers specific for unmethylated target DNA contain T in squares; primers specific for methylated DNA target contain C in squares).

Article Snippet: We describe a novel combination of techniques conferring the sensitivity and specificity of MSP while also benefiting from subsequent validation using pyrosequencing: methylation enrichment pyrosequencing (MEP).

Techniques: Sequencing, Control, Methylation

Tumour characteristics and p16/cyclin A1  methylation  results

Journal: Nucleic Acids Research

Article Title: Methylation enrichment pyrosequencing: combining the specificity of MSP with validation by pyrosequencing

doi: 10.1093/nar/gkl424

Figure Lengend Snippet: Tumour characteristics and p16/cyclin A1 methylation results

Article Snippet: We describe a novel combination of techniques conferring the sensitivity and specificity of MSP while also benefiting from subsequent validation using pyrosequencing: methylation enrichment pyrosequencing (MEP).

Techniques: Methylation

Agarose gels of PCR products following ( a ) p16 MSP, ( b ) p16 MEP, and ( c ) cyclin A1 MEP. U, PCR using MSP primers specific for unmethylated DNA; M, PCR using methylation-specific MSP primers; A and B, two independent MEP assays. Rows 1–4 (top to bottom) correlate with rows 1–4 in dilution matrix ; i.e. row 1, no dilution of starting M:U concentrations; row 2, 1/10 dilutions, etc. Lanes 1–8 correlate with columns 1–8 in dilution matrix ; i.e. lane 1, M:U ratio of 1:1; lane 2, M:U ratio of 1:5, etc.

Journal: Nucleic Acids Research

Article Title: Methylation enrichment pyrosequencing: combining the specificity of MSP with validation by pyrosequencing

doi: 10.1093/nar/gkl424

Figure Lengend Snippet: Agarose gels of PCR products following ( a ) p16 MSP, ( b ) p16 MEP, and ( c ) cyclin A1 MEP. U, PCR using MSP primers specific for unmethylated DNA; M, PCR using methylation-specific MSP primers; A and B, two independent MEP assays. Rows 1–4 (top to bottom) correlate with rows 1–4 in dilution matrix ; i.e. row 1, no dilution of starting M:U concentrations; row 2, 1/10 dilutions, etc. Lanes 1–8 correlate with columns 1–8 in dilution matrix ; i.e. lane 1, M:U ratio of 1:1; lane 2, M:U ratio of 1:5, etc.

Article Snippet: We describe a novel combination of techniques conferring the sensitivity and specificity of MSP while also benefiting from subsequent validation using pyrosequencing: methylation enrichment pyrosequencing (MEP).

Techniques: Methylation

Pyrogram for a typical p16 MEP showing 100% methylation. Shaded bars encompassing T/C pairs, seven interrogated CpG (T, conversion of unmethylated C to U; C, non-conversion of methylated C); box, control, non-CpG cytosine (0% cytosine incorporated). a: Sequence context ATYG. Equal height of T and C peaks at 5 units indicates 100% methylation of C. b: Sequence context GTTYGG. Height of T peak (10 units) is twice the height of C peak (5 units) indicating 100% methylation.

Journal: Nucleic Acids Research

Article Title: Methylation enrichment pyrosequencing: combining the specificity of MSP with validation by pyrosequencing

doi: 10.1093/nar/gkl424

Figure Lengend Snippet: Pyrogram for a typical p16 MEP showing 100% methylation. Shaded bars encompassing T/C pairs, seven interrogated CpG (T, conversion of unmethylated C to U; C, non-conversion of methylated C); box, control, non-CpG cytosine (0% cytosine incorporated). a: Sequence context ATYG. Equal height of T and C peaks at 5 units indicates 100% methylation of C. b: Sequence context GTTYGG. Height of T peak (10 units) is twice the height of C peak (5 units) indicating 100% methylation.

Article Snippet: We describe a novel combination of techniques conferring the sensitivity and specificity of MSP while also benefiting from subsequent validation using pyrosequencing: methylation enrichment pyrosequencing (MEP).

Techniques: Methylation, Control, Sequencing