about
Hybridization-based reconstruction of small non-coding RNA transcripts from deep sequencing data.NGSANE: a lightweight production informatics framework for high-throughput data analysis.A comparative study of techniques for differential expression analysis on RNA-Seq data.Evaluation of computational programs to predict HLA genotypes from genomic sequencing data.STAR: predicting recombination sites from amino acid sequence.Blue: correcting sequencing errors using consensus and context.The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line.Early life events influence whole-of-life metabolic health via gut microflora and gut permeability.Gut permeability, its interaction with gut microflora and effects on metabolic health are mediated by the lymphatics system, liver and bile acid.Genome-wide analysis of chemically induced mutations in mouse in phenotype-driven screensVariantSpark: population scale clustering of genotype information.Cpipe: a shared variant detection pipeline designed for diagnostic settingsTargeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome familiesThree-dimensional disorganization of the cancer genome occurs coincident with long-range genetic and epigenetic alterations.A novel ENU-induced ankyrin-1 mutation impairs parasite invasion and increases erythrocyte clearance during malaria infection in mice.Genomics and personalised whole-of-life healthcare.Sorting the nuclear proteome.Ankyrin-1 Gene Exhibits Allelic Heterogeneity in Conferring Protection Against Malaria.Adenosine monophosphate deaminase 3 activation shortens erythrocyte half-life and provides malaria resistance in mice.The Current State and Future of CRISPR-Cas9 gRNA Design ToolsUnlocking HDR-mediated nucleotide editing by identifying high-efficiency target sites using machine learningMonozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression.High Activity Target-Site Identification Using Phenotypic Independent CRISPR-Cas9 Core FunctionalityMethylome and transcriptome maps of human visceral and subcutaneous adipocytes reveal key epigenetic differences at developmental genesVARSCOT: variant-aware detection and scoring enables sensitive and personalized off-target detection for CRISPR-Cas9Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis
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description
researcher
@en
wetenschapper
@nl
հետազոտող
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name
Denis C Bauer
@ast
Denis C Bauer
@en
Denis C Bauer
@es
Denis C Bauer
@nl
type
label
Denis C Bauer
@ast
Denis C Bauer
@en
Denis C Bauer
@es
Denis C Bauer
@nl
prefLabel
Denis C Bauer
@ast
Denis C Bauer
@en
Denis C Bauer
@es
Denis C Bauer
@nl
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P106
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P2456
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P496
0000-0001-8033-9810