Search Results - "Dyrberg Andersen, Jeppe"
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Comparison of whole transcriptome sequencing of fresh, frozen, and formalin-fixed, paraffin-embedded cardiac tissue
Published in PloS one (29-03-2023)“…The use of fresh tissue for molecular studies is preferred but often impossible. Instead, frozen or formalin-fixed, paraffin-embedded (FFPE) tissues are widely…”
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2
Comparison of global DNA methylation analysis by whole genome bisulfite sequencing and the Infinium Mouse Methylation BeadChip using fresh and fresh-frozen mouse epidermis
Published in Epigenetics (31-12-2023)“…Until recently, studying the murine methylome was restricted to sequencing-based methods. In this study we compared the global DNA methylation levels of…”
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3
Comparison of whole transcriptome sequencing of fresh, frozen, and formalin-fixed, paraffin-embedded cardiac tissue
Published in PloS one (29-03-2023)“…The use of fresh tissue for molecular studies is preferred but often impossible. Instead, frozen or formalin-fixed, paraffin-embedded (FFPE) tissues are widely…”
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4
RYR2 Variant and Sudden Death in Patients With Dilated Cardiomyopathy
Published in Journal of the American College of Cardiology (19-03-2024)Get full text
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5
SNP allele calling of Illumina Infinium Omni5-4 data using the butterfly method
Published in Scientific reports (12-10-2022)“…We introduce a within-sample SNP calling method, called the “butterfly method”, that improves the quality of SNP calling with the Illumina Infinium Omni5-4 SNP…”
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6
Evaluation of DNAmAge in paired fresh, frozen, and formalin-fixed paraffin-embedded heart tissues
Published in PloS one (08-05-2024)“…The continued development in methylome analysis has enabled a more precise assessment of DNA methylation, but treatment of target tissue prior to analysis may…”
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Reproducibility of the Infinium methylationEPIC BeadChip assay using low DNA amounts
Published in Epigenetics (02-12-2022)“…The Infinium MethylationEPIC BeadChip (EPIC) is a reliable method for measuring the DNA methylation of more than 850,000 CpG positions. In clinical and…”
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DNA methylation stability in cardiac tissues kept at different temperatures and time intervals
Published in Scientific reports (24-10-2024)“…Investigating DNA methylation (DNAm) in cardiac tissues is vital for epigenetic research in cardiovascular diseases (CVDs). During cardiac surgery, biopsies…”
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9
Exploratory DNA methylation analysis in post-mortem heart tissue of sudden unexplained death
Published in Clinical epigenetics (22-11-2024)“…Background Sudden unexplained death (SUD) is a devastating event in the young. Despite efforts to identify causal genetic variants, many cases remain…”
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10
Fresh and frozen cardiac tissue are comparable in DNA methylation array β-values, but formalin-fixed, paraffin-embedded tissue may overestimate DNA methylation levels
Published in Scientific reports (29-09-2023)“…Untreated fresh cardiac tissue is the optimal tissue material for investigating DNA methylation patterns of cardiac biology and diseases. However, fresh tissue…”
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11
A comparative study of single nucleotide variant detection performance using three massively parallel sequencing methods
Published in PloS one (28-09-2020)“…Massively parallel sequencing (MPS) has revolutionised clinical genetics and research within human genetics by enabling the detection of variants in multiple…”
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12
Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness
Published in PloS one (22-05-2015)“…Androgenetic alopecia, known in men as male pattern baldness (MPB), is a very conspicuous condition that is particularly frequent among European men and thus…”
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13
Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy
Published in International journal of molecular sciences (10-03-2021)“…Sudden cardiac death (SCD) is a diagnostic challenge in forensic medicine. In a relatively large proportion of the SCDs, the deaths remain unexplained after…”
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14
Sequence variants in muscle tissue‐related genes may determine the severity of muscle contractures in cerebral palsy
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01-01-2019)“…Muscle contractures are a common complication to cerebral palsy (CP). The purpose of this study was to evaluate whether individuals with CP carry specific gene…”
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Pigmentary Markers in Danes--Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma Syndrome
Published in PloS one (03-03-2016)“…To investigate whether pigmentation genes involved in the melanogenic pathway (melanogenesis) contributed to melanoma predisposition, we compared pigmentary…”
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16
Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour
Published in Forensic science international : genetics (01-07-2014)“…Abstract The IrisPlex system is a DNA-based test system for the prediction of human eye colour from biological samples and consists of a single forensically…”
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Identification of individuals from low template blood samples using whole transcriptome shotgun sequencing
Published in Forensic science international : genetics (01-09-2024)“…Biological trace samples consisting of very few cells pose a challenge to conventional forensic genetic DNA analysis. RNA may be an alternative to DNA when…”
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Identification of individuals by RNA sequencing of low template samples
Published in Forensic science international. Genetics supplement series (01-12-2022)“…In this pilot study, we made dilutions of DNA/RNA co-extractions (1000–12.5 pg gDNA) and whole transcriptome shotgun sequenced RNA on a NovaSeq 6000 platform…”
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Altered gene expression levels of genes related to muscle function in adults with cerebral palsy
Published in Tissue & cell (01-06-2022)“…•Significant different gene expression levels were observed between adults with CP and typical developing (TD) adults in various genes.•Differences in muscle…”
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Shotgun DNA sequencing for human identification: Dynamic SNP selection and likelihood ratio calculations accounting for errors
Published in Forensic science international : genetics (01-01-2025)“…Shotgun sequencing is a DNA analysis method that potentially determines the nucleotide sequence of every DNA fragment in a sample, unlike PCR-based genotyping…”
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