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hg002 epiqc bisulfite sequencing methylseq data set  (Epigenomics ag)

 
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    Epigenomics ag hg002 epiqc bisulfite sequencing methylseq data set
    Overall comparison of DNA methylation calls between R9 and R10 data sets across the <t>HG002</t> cell line, blood, and brain samples. ( A ) Methylation proportions of R9 (orange) and R10 (blue) data for the HG002 cell line when binned by bisulfite (green) methylation intervals. The portions of R9 and R10 methylation distributions that agree with the bisulfite methylation range are highlighted in green. ( B–D ) The violin plots underneath show methylation proportions of R9 and R10 data for the HG002 cell line, brain sample, and blood sample binned according to R9 intervals. Each violin plot has lines connecting the median interval points for better visualization of methylation trends. Distributions of CpG site methylation frequencies are depicted on the right side of each panel. ( E ) Stacked bar charts showing the breakdown of total CpG sites per technology per sample. These sites are further subset into CpG sites with 0% methylation frequency and 100% methylation frequency .
    Hg002 Epiqc Bisulfite Sequencing Methylseq Data Set, supplied by Epigenomics ag, 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/hg002+epiqc+bisulfite+sequencing+methylseq+data+set/hg002+epiqc+bisulfite+sequencing+methylseq+data+set/pmc12047266-203-1-25
    Average 90 stars, based on 1 article reviews
    hg002 epiqc bisulfite sequencing methylseq data set - by Bioz Stars, 2026-11
    90/100 stars

    Images

    1) Product Images from "Assessing DNA methylation detection for primary human tissue using Nanopore sequencing"

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing

    Journal: Genome Research

    doi: 10.1101/gr.279159.124

    Overall comparison of DNA methylation calls between R9 and R10 data sets across the HG002 cell line, blood, and brain samples. ( A ) Methylation proportions of R9 (orange) and R10 (blue) data for the HG002 cell line when binned by bisulfite (green) methylation intervals. The portions of R9 and R10 methylation distributions that agree with the bisulfite methylation range are highlighted in green. ( B–D ) The violin plots underneath show methylation proportions of R9 and R10 data for the HG002 cell line, brain sample, and blood sample binned according to R9 intervals. Each violin plot has lines connecting the median interval points for better visualization of methylation trends. Distributions of CpG site methylation frequencies are depicted on the right side of each panel. ( E ) Stacked bar charts showing the breakdown of total CpG sites per technology per sample. These sites are further subset into CpG sites with 0% methylation frequency and 100% methylation frequency .
    Figure Legend Snippet: Overall comparison of DNA methylation calls between R9 and R10 data sets across the HG002 cell line, blood, and brain samples. ( A ) Methylation proportions of R9 (orange) and R10 (blue) data for the HG002 cell line when binned by bisulfite (green) methylation intervals. The portions of R9 and R10 methylation distributions that agree with the bisulfite methylation range are highlighted in green. ( B–D ) The violin plots underneath show methylation proportions of R9 and R10 data for the HG002 cell line, brain sample, and blood sample binned according to R9 intervals. Each violin plot has lines connecting the median interval points for better visualization of methylation trends. Distributions of CpG site methylation frequencies are depicted on the right side of each panel. ( E ) Stacked bar charts showing the breakdown of total CpG sites per technology per sample. These sites are further subset into CpG sites with 0% methylation frequency and 100% methylation frequency .

    Techniques Used: Comparison, DNA Methylation Assay, Methylation

    Genome-wide and regional methylation calling trends in HG002 R9 and R10 data sets. ( A ) Methylation calls for all CpG motifs (strand combined) in HG002 R9 and R10. ( B ) Scatterplot of 2 kb whole-genome windows with a minimum of 10 CpGs for R9 and R10. The 0–100 diagonal line is overlaid in cyan for reference. ( C , D ) Average methylation over the 29,124 filtered human promoters with a minimum of 10 CpGs plotted as a histogram and a scatter plot. ( E,F ) A histogram and scatter plot of the CpG island BED regions with more than 10 CpGs in HG002. All plots are limited to CpG sites with >5× read coverage. The y -axis is log scaled.
    Figure Legend Snippet: Genome-wide and regional methylation calling trends in HG002 R9 and R10 data sets. ( A ) Methylation calls for all CpG motifs (strand combined) in HG002 R9 and R10. ( B ) Scatterplot of 2 kb whole-genome windows with a minimum of 10 CpGs for R9 and R10. The 0–100 diagonal line is overlaid in cyan for reference. ( C , D ) Average methylation over the 29,124 filtered human promoters with a minimum of 10 CpGs plotted as a histogram and a scatter plot. ( E,F ) A histogram and scatter plot of the CpG island BED regions with more than 10 CpGs in HG002. All plots are limited to CpG sites with >5× read coverage. The y -axis is log scaled.

    Techniques Used: Genome Wide, Methylation

    Comparison of HG002 immortalized cell line methylation calling between technologies. ( A ) Methylation proportion histograms for each technology. ( B ) Pairwise site-specific CpG methylation proportion comparison between technologies. ( C ) Site-specific CpG methylation proportion comparison between R10 and bisulfite sequencing. ( D ) RMSE values for pairwise comparisons between technology in Illumina 150 bp paired-end mappable regions as defined by BisMap. ( E ) RMSE for pairwise comparisons between technologies in Illumina 150 bp paired-end hard-to-map regions.
    Figure Legend Snippet: Comparison of HG002 immortalized cell line methylation calling between technologies. ( A ) Methylation proportion histograms for each technology. ( B ) Pairwise site-specific CpG methylation proportion comparison between technologies. ( C ) Site-specific CpG methylation proportion comparison between R10 and bisulfite sequencing. ( D ) RMSE values for pairwise comparisons between technology in Illumina 150 bp paired-end mappable regions as defined by BisMap. ( E ) RMSE for pairwise comparisons between technologies in Illumina 150 bp paired-end hard-to-map regions.

    Techniques Used: Comparison, Methylation, CpG Methylation Assay, Methylation Sequencing

    Haplotype-specific methylation differences and similarities between cell, blood, and brain samples. From top to bottom , each plot shows the genome coordinates, labeled gene models (if present), haplotype-aware read mappings with modified bases as black (methylated), or colored (unmethylated) circles, a smoothed methylation fraction plot, and a coverage plot. The highlighted region corresponds to a 75 bp deletion (Chr16:88,534,247–88,534,321) in haplotype 2 of the HG002 cell line that coincides with haplotype-specific methylation. Coordinates across the bottom refer to methylation bins used in the smoothed methylation plot. ( A ) Haplotype-specific methylation differences and similarities between the R9 and R10 sequenced HG002 cell line. ( B ) Haplotype-specific methylation differences and similarities between the R10 sequenced cell line, blood, and brain samples.
    Figure Legend Snippet: Haplotype-specific methylation differences and similarities between cell, blood, and brain samples. From top to bottom , each plot shows the genome coordinates, labeled gene models (if present), haplotype-aware read mappings with modified bases as black (methylated), or colored (unmethylated) circles, a smoothed methylation fraction plot, and a coverage plot. The highlighted region corresponds to a 75 bp deletion (Chr16:88,534,247–88,534,321) in haplotype 2 of the HG002 cell line that coincides with haplotype-specific methylation. Coordinates across the bottom refer to methylation bins used in the smoothed methylation plot. ( A ) Haplotype-specific methylation differences and similarities between the R9 and R10 sequenced HG002 cell line. ( B ) Haplotype-specific methylation differences and similarities between the R10 sequenced cell line, blood, and brain samples.

    Techniques Used: Methylation, Labeling, Modification

    Related Articles

    Methylation Sequencing:

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing
    Article Snippet: .. The HG002 EpiQC bisulfite sequencing MethylSeq data set used to benchmark the HG002 ONT bisulfite sequencing data set was generated as part of the SEQC2 Epigenomics Quality Control Study ( ). ..

    Generated:

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing
    Article Snippet: .. The HG002 EpiQC bisulfite sequencing MethylSeq data set used to benchmark the HG002 ONT bisulfite sequencing data set was generated as part of the SEQC2 Epigenomics Quality Control Study ( ). ..

    Control:

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing
    Article Snippet: .. The HG002 EpiQC bisulfite sequencing MethylSeq data set used to benchmark the HG002 ONT bisulfite sequencing data set was generated as part of the SEQC2 Epigenomics Quality Control Study ( ). ..



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    Epigenomics ag hg002 epiqc bisulfite sequencing methylseq data set
    Overall comparison of DNA methylation calls between R9 and R10 data sets across the <t>HG002</t> cell line, blood, and brain samples. ( A ) Methylation proportions of R9 (orange) and R10 (blue) data for the HG002 cell line when binned by bisulfite (green) methylation intervals. The portions of R9 and R10 methylation distributions that agree with the bisulfite methylation range are highlighted in green. ( B–D ) The violin plots underneath show methylation proportions of R9 and R10 data for the HG002 cell line, brain sample, and blood sample binned according to R9 intervals. Each violin plot has lines connecting the median interval points for better visualization of methylation trends. Distributions of CpG site methylation frequencies are depicted on the right side of each panel. ( E ) Stacked bar charts showing the breakdown of total CpG sites per technology per sample. These sites are further subset into CpG sites with 0% methylation frequency and 100% methylation frequency .
    Hg002 Epiqc Bisulfite Sequencing Methylseq Data Set, supplied by Epigenomics ag, 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/hg002+epiqc+bisulfite+sequencing+methylseq+data+set/hg002+epiqc+bisulfite+sequencing+methylseq+data+set/pmc12047266-203-1-25
    Average 90 stars, based on 1 article reviews
    hg002 epiqc bisulfite sequencing methylseq data set - by Bioz Stars, 2026-11
    90/100 stars
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    Overall comparison of DNA methylation calls between R9 and R10 data sets across the HG002 cell line, blood, and brain samples. ( A ) Methylation proportions of R9 (orange) and R10 (blue) data for the HG002 cell line when binned by bisulfite (green) methylation intervals. The portions of R9 and R10 methylation distributions that agree with the bisulfite methylation range are highlighted in green. ( B–D ) The violin plots underneath show methylation proportions of R9 and R10 data for the HG002 cell line, brain sample, and blood sample binned according to R9 intervals. Each violin plot has lines connecting the median interval points for better visualization of methylation trends. Distributions of CpG site methylation frequencies are depicted on the right side of each panel. ( E ) Stacked bar charts showing the breakdown of total CpG sites per technology per sample. These sites are further subset into CpG sites with 0% methylation frequency and 100% methylation frequency .

    Journal: Genome Research

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing

    doi: 10.1101/gr.279159.124

    Figure Lengend Snippet: Overall comparison of DNA methylation calls between R9 and R10 data sets across the HG002 cell line, blood, and brain samples. ( A ) Methylation proportions of R9 (orange) and R10 (blue) data for the HG002 cell line when binned by bisulfite (green) methylation intervals. The portions of R9 and R10 methylation distributions that agree with the bisulfite methylation range are highlighted in green. ( B–D ) The violin plots underneath show methylation proportions of R9 and R10 data for the HG002 cell line, brain sample, and blood sample binned according to R9 intervals. Each violin plot has lines connecting the median interval points for better visualization of methylation trends. Distributions of CpG site methylation frequencies are depicted on the right side of each panel. ( E ) Stacked bar charts showing the breakdown of total CpG sites per technology per sample. These sites are further subset into CpG sites with 0% methylation frequency and 100% methylation frequency .

    Article Snippet: The HG002 EpiQC bisulfite sequencing MethylSeq data set used to benchmark the HG002 ONT bisulfite sequencing data set was generated as part of the SEQC2 Epigenomics Quality Control Study ( ).

    Techniques: Comparison, DNA Methylation Assay, Methylation

    Genome-wide and regional methylation calling trends in HG002 R9 and R10 data sets. ( A ) Methylation calls for all CpG motifs (strand combined) in HG002 R9 and R10. ( B ) Scatterplot of 2 kb whole-genome windows with a minimum of 10 CpGs for R9 and R10. The 0–100 diagonal line is overlaid in cyan for reference. ( C , D ) Average methylation over the 29,124 filtered human promoters with a minimum of 10 CpGs plotted as a histogram and a scatter plot. ( E,F ) A histogram and scatter plot of the CpG island BED regions with more than 10 CpGs in HG002. All plots are limited to CpG sites with >5× read coverage. The y -axis is log scaled.

    Journal: Genome Research

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing

    doi: 10.1101/gr.279159.124

    Figure Lengend Snippet: Genome-wide and regional methylation calling trends in HG002 R9 and R10 data sets. ( A ) Methylation calls for all CpG motifs (strand combined) in HG002 R9 and R10. ( B ) Scatterplot of 2 kb whole-genome windows with a minimum of 10 CpGs for R9 and R10. The 0–100 diagonal line is overlaid in cyan for reference. ( C , D ) Average methylation over the 29,124 filtered human promoters with a minimum of 10 CpGs plotted as a histogram and a scatter plot. ( E,F ) A histogram and scatter plot of the CpG island BED regions with more than 10 CpGs in HG002. All plots are limited to CpG sites with >5× read coverage. The y -axis is log scaled.

    Article Snippet: The HG002 EpiQC bisulfite sequencing MethylSeq data set used to benchmark the HG002 ONT bisulfite sequencing data set was generated as part of the SEQC2 Epigenomics Quality Control Study ( ).

    Techniques: Genome Wide, Methylation

    Comparison of HG002 immortalized cell line methylation calling between technologies. ( A ) Methylation proportion histograms for each technology. ( B ) Pairwise site-specific CpG methylation proportion comparison between technologies. ( C ) Site-specific CpG methylation proportion comparison between R10 and bisulfite sequencing. ( D ) RMSE values for pairwise comparisons between technology in Illumina 150 bp paired-end mappable regions as defined by BisMap. ( E ) RMSE for pairwise comparisons between technologies in Illumina 150 bp paired-end hard-to-map regions.

    Journal: Genome Research

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing

    doi: 10.1101/gr.279159.124

    Figure Lengend Snippet: Comparison of HG002 immortalized cell line methylation calling between technologies. ( A ) Methylation proportion histograms for each technology. ( B ) Pairwise site-specific CpG methylation proportion comparison between technologies. ( C ) Site-specific CpG methylation proportion comparison between R10 and bisulfite sequencing. ( D ) RMSE values for pairwise comparisons between technology in Illumina 150 bp paired-end mappable regions as defined by BisMap. ( E ) RMSE for pairwise comparisons between technologies in Illumina 150 bp paired-end hard-to-map regions.

    Article Snippet: The HG002 EpiQC bisulfite sequencing MethylSeq data set used to benchmark the HG002 ONT bisulfite sequencing data set was generated as part of the SEQC2 Epigenomics Quality Control Study ( ).

    Techniques: Comparison, Methylation, CpG Methylation Assay, Methylation Sequencing

    Haplotype-specific methylation differences and similarities between cell, blood, and brain samples. From top to bottom , each plot shows the genome coordinates, labeled gene models (if present), haplotype-aware read mappings with modified bases as black (methylated), or colored (unmethylated) circles, a smoothed methylation fraction plot, and a coverage plot. The highlighted region corresponds to a 75 bp deletion (Chr16:88,534,247–88,534,321) in haplotype 2 of the HG002 cell line that coincides with haplotype-specific methylation. Coordinates across the bottom refer to methylation bins used in the smoothed methylation plot. ( A ) Haplotype-specific methylation differences and similarities between the R9 and R10 sequenced HG002 cell line. ( B ) Haplotype-specific methylation differences and similarities between the R10 sequenced cell line, blood, and brain samples.

    Journal: Genome Research

    Article Title: Assessing DNA methylation detection for primary human tissue using Nanopore sequencing

    doi: 10.1101/gr.279159.124

    Figure Lengend Snippet: Haplotype-specific methylation differences and similarities between cell, blood, and brain samples. From top to bottom , each plot shows the genome coordinates, labeled gene models (if present), haplotype-aware read mappings with modified bases as black (methylated), or colored (unmethylated) circles, a smoothed methylation fraction plot, and a coverage plot. The highlighted region corresponds to a 75 bp deletion (Chr16:88,534,247–88,534,321) in haplotype 2 of the HG002 cell line that coincides with haplotype-specific methylation. Coordinates across the bottom refer to methylation bins used in the smoothed methylation plot. ( A ) Haplotype-specific methylation differences and similarities between the R9 and R10 sequenced HG002 cell line. ( B ) Haplotype-specific methylation differences and similarities between the R10 sequenced cell line, blood, and brain samples.

    Article Snippet: The HG002 EpiQC bisulfite sequencing MethylSeq data set used to benchmark the HG002 ONT bisulfite sequencing data set was generated as part of the SEQC2 Epigenomics Quality Control Study ( ).

    Techniques: Methylation, Labeling, Modification