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We reviewed 3 live results for epigenomics and narrowed them down to the 3 options that look most worth comparing first.
The options are Epigenomics Sequencing Service, Infinium Methylation Screening Array-48 Kit and WGBS (Whole Genome Bisulfite Sequencing) and EM-seq (Enzymatic Methylation) Service.
Source: CD Genomics
Description
CD Genomics provides advanced epigenomics sequencing and bioinformatics services to decode gene regulatory networks for research applications in cancer, developmental biology, neurobiology, aging, and drug discovery. Its portfolio includes genome-wide and targeted DNA methylation analysis, DNA hydroxymethylation, RNA modification profiling, chromatin accessibility assays such as ATAC-Seq and ChIP-Seq, and cell-free DNA methylation. Utilizing platforms like Illumina NovaSeq 6000, Oxford Nanopore MinION, and 10x Genomics Chromium, the service covers sample detection, library construction, sequencing execution, and detailed bioinformatics reporting.
Best for
Life science researchers, Genomics and oncology investigators, Epigenetic biomarker discovery and Investigating gene regulation mechanisms
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Source: Illumina
Description
The Infinium Methylation Screening Array-48 Kit is a scalable, high-throughput DNA methylation microarray designed for population health research and large-scale association studies. Profiling approximately 270K unique methylation sites across 48 samples per BeadChip, it utilizes the Infinium EX Methylation assay on the iScan System with low 50 ng DNA input requirements.
Best for
population health researchers, epigenetics researchers, large-scale epigenome-wide association studies (EWAS) and biobank screening projects
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Source: Diagenode
Description
Diagenode provides comprehensive WGBS (Whole Genome Bisulfite Sequencing) and EM-seq (Enzymatic Methylation) services for in-depth, genome-wide DNA methylation profiling at single-nucleotide resolution. The end-to-end workflow spans genomic DNA quality control, library preparation, and deep paired-end sequencing on Illumina platforms, detecting over 50 million CpGs across human, mouse, and rat samples. It supports low input, cfDNA, and FFPE specimens, with dedicated scientist guidance and optional bioinformatics analysis including differential methylation, pathway analysis, and biomarker data mining.
Best for
epigenomics researchers, biomarker discovery scientists, genome-wide DNA methylation profiling and single-nucleotide resolution epigenetic analysis
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| Compare | #1Epigenomics Sequencing Service | #2Infinium Methylation Screening Array-48 Kit | #3WGBS (Whole Genome Bisulfite Sequencing) and EM-seq (Enzymatic Methylation) Service |
|---|---|---|---|
| Source | CD Genomics | Illumina | Diagenode |
| Description | CD Genomics provides advanced epigenomics sequencing and bioinformatics services to decode gene regulatory networks for research applications in cancer, developmental biology, neurobiology, aging, and drug discovery. Its portfolio includes genome-wide and targeted DNA methylation analysis, DNA hydroxymethylation, RNA modification profiling, chromatin accessibility assays such as ATAC-Seq and ChIP-Seq, and cell-free DNA methylation. Utilizing platforms like Illumina NovaSeq 6000, Oxford Nanopore MinION, and 10x Genomics Chromium, the service covers sample detection, library construction, sequencing execution, and detailed bioinformatics reporting. | The Infinium Methylation Screening Array-48 Kit is a scalable, high-throughput DNA methylation microarray designed for population health research and large-scale association studies. Profiling approximately 270K unique methylation sites across 48 samples per BeadChip, it utilizes the Infinium EX Methylation assay on the iScan System with low 50 ng DNA input requirements. | Diagenode provides comprehensive WGBS (Whole Genome Bisulfite Sequencing) and EM-seq (Enzymatic Methylation) services for in-depth, genome-wide DNA methylation profiling at single-nucleotide resolution. The end-to-end workflow spans genomic DNA quality control, library preparation, and deep paired-end sequencing on Illumina platforms, detecting over 50 million CpGs across human, mouse, and rat samples. It supports low input, cfDNA, and FFPE specimens, with dedicated scientist guidance and optional bioinformatics analysis including differential methylation, pathway analysis, and biomarker data mining. |
| Best for | Life science researchers, Genomics and oncology investigators, Epigenetic biomarker discovery and Investigating gene regulation mechanisms | population health researchers, epigenetics researchers, large-scale epigenome-wide association studies (EWAS) and biobank screening projects | epigenomics researchers, biomarker discovery scientists, genome-wide DNA methylation profiling and single-nucleotide resolution epigenetic analysis |
| Action | CD Genomics | Illumina | Diagenode |
| Rate this product |
"Epigenomics Sequencing Service from CD Genomics."
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