Spark: a navigational paradigm for genomic data exploration. Read more about Spark: a navigational paradigm for genomic data exploration.
Human genomic disease variants: a neutral evolutionary explanation. Read more about Human genomic disease variants: a neutral evolutionary explanation.
Coding exons function as tissue-specific enhancers of nearby genes. Read more about Coding exons function as tissue-specific enhancers of nearby genes.
A DNA hypermethylation module for the stem/progenitor cell signature of cancer. Read more about A DNA hypermethylation module for the stem/progenitor cell signature of cancer.
Whole genome sequencing of matched primary and metastatic acral melanomas. Read more about Whole genome sequencing of matched primary and metastatic acral melanomas.
Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition. Read more about Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition.
Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience. Read more about Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience.
DNA methylation profiling reveals novel biomarkers and important roles for DNA methyltransferases in prostate cancer. Read more about DNA methylation profiling reveals novel biomarkers and important roles for DNA methyltransferases in prostate cancer.
Neurons show distinctive DNA methylation profile and higher interindividual variations compared with non-neurons. Read more about Neurons show distinctive DNA methylation profile and higher interindividual variations compared with non-neurons.
Coevolution within a transcriptional network by compensatory trans and cis mutations. Read more about Coevolution within a transcriptional network by compensatory trans and cis mutations.
