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Nucleic Acids Research|July 14, 2016
Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseasesYue Li, Manolis KellisAmerican Journal of Human Genetics|October 27, 2023
Power of inclusion: Enhancing polygenic prediction with admixed individualsYosuke Tanigawa, Manolis KellisNature Communications|August 19, 2015
Systematic chromatin state comparison of epigenomes associated with diverse properties including sex and tissue typeAngela Yen, Manolis KellisPlos Computational Biology|March 26, 2013
RFECS: a random-forest based algorithm for enhancer identification from chromatin stateNisha Rajagopal, Wei Xie, Yan Li, et al.Genome Research|March 21, 2013
Systematic dissection of regulatory motifs in 2000 predicted human enhancers using a massively parallel reporter assayPouya Kheradpour, Jason Ernst, Alexandre Melnikov, et al.Genome Biology|March 19, 2005
Large-scale discovery and validation of functional elements in the human genomeBradley E Bernstein, Manolis KellisNucleic Acids Research|November 9, 2011
HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variantsLucas D Ward, Manolis KellisGenome Research|January 25, 2012
Unified modeling of gene duplication, loss, and coalescence using a locus treeMatthew D Rasmussen, Manolis KellisScience (New York, N.Y.)|May 11, 2013
Response to comment on "Evidence of abundant purifying selection in humans for recently acquired regulatory functions"Lucas D Ward, Manolis KellisScience (New York, N.Y.)|September 8, 2012
Evidence of abundant purifying selection in humans for recently acquired regulatory functionsLucas D Ward, Manolis KellisPageof 40