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Search Results to Tomi Pastinen

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One or more keywords matched the following properties of Pastinen, Tomi

keywords Genomics

One or more keywords matched the following items that are connected to Pastinen, Tomi

Item TypeName
Academic Article A survey of genetic and epigenetic variation affecting human gene expression.
Academic Article Mapping cis-acting regulatory variation in recombinant congenic strains.
Academic Article Systematic assessment of the human osteoblast transcriptome in resting and induced primary cells.
Academic Article Population genomics in a disease targeted primary cell model.
Academic Article Genome-wide allele-specific analysis: insights into regulatory variation.
Academic Article Computational analysis of whole-genome differential allelic expression data in human.
Academic Article Genome-wide assessment of imprinted expression in human cells.
Academic Article Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.
Academic Article Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Academic Article Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells.
Academic Article Optimizing ChIP-seq peak detectors using visual labels and supervised machine learning.
Academic Article Are Data Sharing and Privacy Protection Mutually Exclusive?
Academic Article Conserved expression of transposon-derived non-coding transcripts in primate stem cells.
Academic Article Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation.
Academic Article Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in na?ve CD4+ T cells.
Academic Article Paired rRNA-depleted and polyA-selected RNA sequencing data and supporting multi-omics data from human T cells.
Academic Article Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Academic Article Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients.
Academic Article The post-diagnostics world: charting a path for pediatric genomic medicine in the twenty-first century.
Academic Article Insurance denials and diagnostic rates in a pediatric genomic research cohort.

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  • Genomics