Loss of epigenetic suppression of retrotransposons with oncogenic potential in aging mammary luminal epithelial cells. Read more about Loss of epigenetic suppression of retrotransposons with oncogenic potential in aging mammary luminal epithelial cells.
A massively parallel 3' UTR reporter assay reveals relationships between nucleotide content, sequence conservation, and mRNA destabilization. Read more about A massively parallel 3' UTR reporter assay reveals relationships between nucleotide content, sequence conservation, and mRNA destabilization.
Transcriptional fates of human-specific segmental duplications in brain. Read more about Transcriptional fates of human-specific segmental duplications in brain.
Tracing human stem cell lineage during development using DNA methylation. Read more about Tracing human stem cell lineage during development using DNA methylation.
Corrigendum: A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity. Read more about Corrigendum: A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity.
Whole-genome sequencing of Atacama skeleton shows novel mutations linked with dysplasia. Read more about Whole-genome sequencing of Atacama skeleton shows novel mutations linked with dysplasia.
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Read more about Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.
A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity. Read more about A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity.
Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants. Read more about Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants.
