The majority of trait associated variants found in GWAS studies lie within non coding sequences. This suggests that a large proportion of variants alter regulatory regions. Certain genomic features has been shown useful as marks of cell type specific activity of genomic regions. Analyzing such genomic features against variant regions may therefore be used to find previously unknown links between trait and cell type. Although there have been done several investigations of this type, no easily accessible tools for this type of research exists. This makes reproduction of such results difficult and time consuming, hindering confirmation and updates of such results Such an accessible tool for studying cell-type specificity of genomic regions is...
<div><p>Genetic variants in cis-regulatory elements or trans-acting regulators frequently influence ...
The human body is composed of hundreds of specialized cell types, each fulfilling distinct functions...
Heritability enrichment analyses pertaining to the sclinker paper (Jagadeesh, Dey et al 2022, in pre...
Summary: Genome-wide association studies (GWASs) have identified hundreds of thousands of genetic va...
Single-cell RNA sequencing (scRNA-seq) data allows to create cell type specific transcriptome profil...
Single-cell sequencing (scRNA-seq) has enabled researchers to study cellular heterogeneity. Accurate...
To understand complex genetic diseases it is necessary to study DNA, its transcription, translation ...
INTRODUCTION: Efforts to map quantitative trait loci (QTLs) across human tissues by the GTEx Consort...
Induced pluripotent stem cells (iPSCs) are an essential tool for studying cellular differentiation a...
[[abstract]]Single nucleotide polymorphisms (SNPs) and short tandem repeats (STRs) are the most comm...
Genetic variants in cis-regulatory elements or trans-acting regulators frequently influence the quan...
Overlap between non-coding DNA regulatory sequences and common variant associations can help to iden...
Background: In cell differentiation, a cell of a less specialized type becomes one of a more special...
AbstractGenome-wide association studies (GWASs) have shown a large number of genetic variants to be ...
Overlap between non-coding DNA regulatory sequences and common variant associations can help to iden...
<div><p>Genetic variants in cis-regulatory elements or trans-acting regulators frequently influence ...
The human body is composed of hundreds of specialized cell types, each fulfilling distinct functions...
Heritability enrichment analyses pertaining to the sclinker paper (Jagadeesh, Dey et al 2022, in pre...
Summary: Genome-wide association studies (GWASs) have identified hundreds of thousands of genetic va...
Single-cell RNA sequencing (scRNA-seq) data allows to create cell type specific transcriptome profil...
Single-cell sequencing (scRNA-seq) has enabled researchers to study cellular heterogeneity. Accurate...
To understand complex genetic diseases it is necessary to study DNA, its transcription, translation ...
INTRODUCTION: Efforts to map quantitative trait loci (QTLs) across human tissues by the GTEx Consort...
Induced pluripotent stem cells (iPSCs) are an essential tool for studying cellular differentiation a...
[[abstract]]Single nucleotide polymorphisms (SNPs) and short tandem repeats (STRs) are the most comm...
Genetic variants in cis-regulatory elements or trans-acting regulators frequently influence the quan...
Overlap between non-coding DNA regulatory sequences and common variant associations can help to iden...
Background: In cell differentiation, a cell of a less specialized type becomes one of a more special...
AbstractGenome-wide association studies (GWASs) have shown a large number of genetic variants to be ...
Overlap between non-coding DNA regulatory sequences and common variant associations can help to iden...
<div><p>Genetic variants in cis-regulatory elements or trans-acting regulators frequently influence ...
The human body is composed of hundreds of specialized cell types, each fulfilling distinct functions...
Heritability enrichment analyses pertaining to the sclinker paper (Jagadeesh, Dey et al 2022, in pre...