Cis-regulatory variation: significance in biomedicine and evolution.

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Imputation for transcription factor binding predictions based on deep learning Towards a map of cis-regulatory sequences in the human genome.

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Cis-regulatory variation: significance in biomedicine and evolution.

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Cis-regulatory variation: significance in biomedicine and evolution.

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Cis-regulatory variation: significance in biomedicine and evolution.

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Cis-regulatory variation: significance in biomedicine and evolution.

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Cis-regulatory variation: significance in biomedicine and evolution.

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Ritwick Sawarkar

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Simon Friedensohn

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Analysis of variation at transcription factor binding sites in Drosophila and humans

Chromatin landscape dictates HSF binding to target DNA elements

DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

An integrated encyclopedia of DNA elements in the human genome

An integrated map of genetic variation from 1,092 human genomes

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Common genetic variants account for differences in gene expression among ethnic groups

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

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s00441-014-1855-3

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495-505

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scholarly article

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10.1007/S00441-014-1855-3

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2014-04-18T00:00:00Z

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Cis-regulatory variation: significance in biomedicine and evolution.

about

P2860

P2860

Cis-regulatory variation: significance in biomedicine and evolution.

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