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Andrew J. Hill

Researcher at University of Washington

Publications -  28
Citations -  17246

Andrew J. Hill is an academic researcher from University of Washington. The author has contributed to research in topics: Gene & Chromatin. The author has an hindex of 17, co-authored 27 publications receiving 13389 citations. Previous affiliations of Andrew J. Hill include Harvard University & Broad Institute.

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Analysis of protein-coding genetic variation in 60,706 humans

Monkol Lek, +106 more
- 18 Aug 2016 - 
TL;DR: The aggregation and analysis of high-quality exome (protein-coding region) DNA sequence data for 60,706 individuals of diverse ancestries generated as part of the Exome Aggregation Consortium (ExAC) provides direct evidence for the presence of widespread mutational recurrence.
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The single-cell transcriptional landscape of mammalian organogenesis

TL;DR: A cell atlas of mouse organogenesis provides a global view of developmental processes occurring during this critical period, including focused analyses of the apical ectodermal ridge, limb mesenchyme and skeletal muscle.
Posted ContentDOI

Analysis of protein-coding genetic variation in 60,706 humans

Monkol Lek, +72 more
- 30 Oct 2015 - 
TL;DR: The aggregation and analysis of high-quality exome (protein-coding region) sequence data for 60,706 individuals of diverse ethnicities generated as part of the Exome Aggregation Consortium (ExAC) provides direct evidence for the presence of widespread mutational recurrence.
Journal ArticleDOI

Single-cell mRNA quantification and differential analysis with Census

TL;DR: The Census algorithm is introduced to convert relative RNA-seq expression levels into relative transcript counts without the need for experimental spike-in controls and it is demonstrated that Census enabled robust analysis at multiple layers of gene regulation.
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Cell-free DNA Comprises an in Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin

TL;DR: Nucleosome spacing inferred from cfDNA in healthy individuals correlates most strongly with epigenetic features of lymphoid and myeloid cells, consistent with hematopoietic cell death as the normal source of cfDNA.