Michael P. Snyder

Microtubule capture by the cleavage apparatus is required for proper spindle positioning in yeast.

Landscape of next-generation sequencing technologies.

A comprehensive map of mobile element insertion polymorphisms in humans.

A core erythroid transcriptional network is repressed by a master regulator of myelo-lymphoid differentiation.

Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype.

Tcf7 is an important regulator of the switch of self-renewal and differentiation in a multipotential hematopoietic cell line.

Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.

Extensive genetic variation in somatic human tissues.

SeqFold: genome-scale reconstruction of RNA secondary structure integrating high-throughput sequencing data.

Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data.

The variable somatic genome.

Two methods for full-length RNA sequencing for low quantities of cells and single cells.

High-throughput sequencing for biology and medicine.

Overview of high throughput sequencing technologies to elucidate molecular pathways in cardiovascular diseases.

Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration.

Impacts of variation in the human genome on gene regulation.

Haplotype structure and positive selection at TLR1.

Defective sphingosine 1-phosphate receptor 1 (S1P1) phosphorylation exacerbates TH17-mediated autoimmune neuroinflammation.

Specific plasma autoantibody reactivity in myelodysplastic syndromes.

Landscape and variation of RNA secondary structure across the human transcriptome.

Divergence in a master variator generates distinct phenotypes and transcriptional responses.

Extended lifespan and reduced adiposity in mice lacking the FAT10 gene.

Quantitative analysis of RNA-protein interactions on a massively parallel array reveals biophysical and evolutionary landscapes.

Defining functional DNA elements in the human genome.

Sushi.R: flexible, quantitative and integrative genomic visualizations for publication-quality multi-panel figures.

Defining a personal, allele-specific, and single-molecule long-read transcriptome.

H3K4me3 breadth is linked to cell identity and transcriptional consistency.

Genomic analysis of fibrolamellar hepatocellular carcinoma.

Shared functions of plant and mammalian StAR-related lipid transfer (START) domains in modulating transcription factor activity.

Genome-wide map of regulatory interactions in the human genome.

Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease.

Widespread contribution of transposable elements to the innovation of gene regulatory networks.

A comparative encyclopedia of DNA elements in the mouse genome.

Principles of regulatory information conservation between mouse and human.

Topologically associating domains are stable units of replication-timing regulation.

Comparison of the transcriptional landscapes between human and mouse tissues.

Personalized sequencing and the future of medicine: discovery, diagnosis and defeat of disease.

Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.

Comprehensive transcriptome analysis using synthetic long-read sequencing reveals molecular co-association of distant splicing events.

High-throughput sequencing technologies.

Transcriptome Signature and Regulation in Human Somatic Cell Reprogramming.

Mango: a bias-correcting ChIA-PET analysis pipeline.

Single-cell chromatin accessibility reveals principles of regulatory variation.