Connection

Search Results to Tomi Pastinen

This is a "connection" page, showing the details of why an item matched the keywords from your search.

Search Results

Pastinen, Tomi

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

Item Type	Name
Concept	Sequence Analysis
Concept	Sequence Analysis, DNA
Concept	Sequence Analysis, RNA
Concept	Oligonucleotide Array Sequence Analysis
Academic Article	Multiplex, fluorescent, solid-phase minisequencing for efficient screening of DNA sequence variation.
Academic Article	Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays.
Academic Article	Contribution of the CCR5 and MBL genes to susceptibility to HIV type 1 infection in the Finnish population.
Academic Article	A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays.
Academic Article	Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays.
Academic Article	A survey of genetic and epigenetic variation affecting human gene expression.
Academic Article	The effect of polymorphisms in the enhancer of split gene complex on bristle number variation in a large wild-caught cohort of Drosophila melanogaster.
Academic Article	Survey of allelic expression using EST mining.
Academic Article	Mapping cis-acting regulatory variation in recombinant congenic strains.
Academic Article	A probabilistic approach for SNP discovery in high-throughput human resequencing data.
Academic Article	Population genomics in a disease targeted primary cell model.
Academic Article	Analysis of the impact of genetic variation on human gene expression.
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	The study of eQTL variations by RNA-seq: from SNPs to phenotypes.
Academic Article	RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression.
Academic Article	Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
Academic Article	Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines.
Academic Article	Genotype-based test in mapping cis-regulatory variants from allele-specific expression data.
Academic Article	The relationship between DNA methylation, genetic and expression inter-individual variation in untransformed human fibroblasts.
Academic Article	Epigenome data release: a participant-centered approach to privacy protection.
Academic Article	Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Academic Article	funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types.
Academic Article	An evaluation of methods correcting for cell-type heterogeneity in DNA methylation studies.
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	A hidden markov model for identifying differentially methylated sites in bisulfite sequencing data.
Academic Article	Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.
Academic Article	Rheumatoid arthritis-relevant DNA methylation changes identified in ACPA-positive asymptomatic individuals using methylome capture sequencing.
Academic Article	A novel statistical method for modeling covariate effects in bisulfite sequencing derived measures of DNA methylation.
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	Comprehensive SMN1 and SMN2 profiling for spinal muscular atrophy analysis using long-read PacBio HiFi sequencing.
Academic Article	Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort.
Academic Article	Case of CLPB deficiency solved by HiFi long read genome sequencing and RNAseq.

Search Criteria

Sequence Analysis