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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 9, 2017
Prediction of protein-ligand interactions from paired protein sequence motifs and ligand substructures
Peyton Greenside, Maureen Hillenmeyer, Anshul Kundaje
Bioinformatics (Oxford, England)
|
November 14, 2018
Discovering epistatic feature interactions from neural network models of regulatory DNA sequences
Peyton Greenside, Tyler Shimko, Polly Fordyce, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
March 14, 2019
CrowdVariant: a crowdsourcing approach to classify copy number variants
Peyton Greenside, Justin Zook, Marc Salit, et al.
Plos One
|
June 18, 2019
Deciphering regulatory DNA sequences and noncoding genetic variants using neural network models of massively parallel reporter assays
Rajiv Movva, Peyton Greenside, Georgi K Marinov, et al.
Nature
|
July 31, 2020
Landscape of cohesin-mediated chromatin loops in the human genome
Fabian Grubert, Rohith Srivas, Damek V Spacek, et al.
Genome Research
|
December 7, 2017
Impact of regulatory variation across human iPSCs and differentiated cells
Nicholas E Banovich, Yang I Li, Anil Raj, et al.
Cell
|
August 25, 2015
Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions
Fabian Grubert, Judith B Zaugg, Maya Kasowski, et al.
Cell
|
December 2, 2017
A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles
Aravind Subramanian, Rajiv Narayan, Steven M Corsello, et al.
Nature Genetics
|
December 5, 2018
Discovery of common and rare genetic risk variants for colorectal cancer
Jeroen R Huyghe, Stephanie A Bien, Tabitha A Harrison, et al.
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Search research articles
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Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 9, 2017
Prediction of protein-ligand interactions from paired protein sequence motifs and ligand substructures
Peyton Greenside, Maureen Hillenmeyer, Anshul Kundaje
Bioinformatics (Oxford, England)
|
November 14, 2018
Discovering epistatic feature interactions from neural network models of regulatory DNA sequences
Peyton Greenside, Tyler Shimko, Polly Fordyce, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
March 14, 2019
CrowdVariant: a crowdsourcing approach to classify copy number variants
Peyton Greenside, Justin Zook, Marc Salit, et al.
Plos One
|
June 18, 2019
Deciphering regulatory DNA sequences and noncoding genetic variants using neural network models of massively parallel reporter assays
Rajiv Movva, Peyton Greenside, Georgi K Marinov, et al.
Nature
|
July 31, 2020
Landscape of cohesin-mediated chromatin loops in the human genome
Fabian Grubert, Rohith Srivas, Damek V Spacek, et al.
Genome Research
|
December 7, 2017
Impact of regulatory variation across human iPSCs and differentiated cells
Nicholas E Banovich, Yang I Li, Anil Raj, et al.
Cell
|
August 25, 2015
Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions
Fabian Grubert, Judith B Zaugg, Maya Kasowski, et al.
Cell
|
December 2, 2017
A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles
Aravind Subramanian, Rajiv Narayan, Steven M Corsello, et al.
Nature Genetics
|
December 5, 2018
Discovery of common and rare genetic risk variants for colorectal cancer
Jeroen R Huyghe, Stephanie A Bien, Tabitha A Harrison, et al.
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