about
Direct observation of base-pair stepping by RNA polymeraseTransient acquisition of pluripotency during somatic cell transdifferentiation with iPSC reprogramming factors.Pulling out the 1%: whole-genome capture for the targeted enrichment of ancient DNA sequencing librariesNfib Promotes Metastasis through a Widespread Increase in Chromatin Accessibility.High-resolution, single-molecule measurements of biomolecular motion.Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy.An optical apparatus for rotation and trapping.Genome-scale measurement of off-target activity using Cas9 toxicity in high-throughput screensHiChIP: efficient and sensitive analysis of protein-directed genome architecture.ATAC-see reveals the accessible genome by transposase-mediated imaging and sequencing.Variable chromatin structure revealed by in situ spatially correlated DNA cleavage mapping.A pause sequence enriched at translation start sites drives transcription dynamics in vivoA conditional system to specifically link disruption of protein-coding function with reporter expression in miceTransposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome positionStructured nucleosome fingerprints enable high-resolution mapping of chromatin architecture within regulatory regions.ATAC-seq: A Method for Assaying Chromatin Accessibility Genome-Wide.Molecule by molecule, the physics and chemistry of life: SMB 2007.Individuality and variation of personal regulomes in primary human T cells.Fluorogenic DNA sequencing in PDMS microreactors.High-throughput biochemical profiling reveals sequence determinants of dCas9 off-target binding and unbinding.Single-cell chromatin accessibility reveals principles of regulatory variationIdentification of significantly mutated regions across cancer types highlights a rich landscape of functional molecular alterationsDirect observation of hierarchical folding in single riboswitch aptamers.Single-molecule studies of RNA polymerase: motoring alongLineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution.Single-cell epigenomic variability reveals functional cancer heterogeneity.Landscape of monoallelic DNA accessibility in mouse embryonic stem cells and neural progenitor cellsAssaying the epigenome in limited numbers of cellsAn improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues.Unraveling the 3D genome: genomics tools for multiscale exploration.chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data.Quantitative analysis of RNA-protein interactions on a massively parallel array reveals biophysical and evolutionary landscapes.Beyond the Linear Genome: Paired-End Sequencing as a Biophysical ToolComprehensive and quantitative mapping of RNA-protein interactions across a transcribed eukaryotic genome.Single-molecule, motion-based DNA sequencing using RNA polymerase.Applied force reveals mechanistic and energetic details of transcription termination.TOP2 synergizes with BAF chromatin remodeling for both resolution and formation of facultative heterochromatin.The future of sequencing: convergence of intelligent design and market Darwinism.Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements.Epigenomics of human CD8 T cell differentiation and aging.
P50
Q24540192-D5E988A0-0F36-4C40-822C-0D4D60AC54ADQ27314024-A53BF76B-FB7D-40C0-97B9-81F8FF537B69Q28661678-62248BF9-FEAA-4A9E-83CE-843E3C90E386Q30276428-BDBF9784-D396-4255-B0B6-142340A579DAQ30501806-950C4344-E420-41C5-99EF-B5CE1104159BQ33581928-72E91910-AFE3-4448-B65E-27AEBA45237FQ33631863-1BFEA5A2-C71A-4041-82C1-185C7E95A5EAQ33654299-38D34E27-113F-4CA7-B2BB-0CCA5BCFD27FQ33883075-31536601-62AF-46E9-BAEA-83DD590FD840Q33902636-FD281E05-C65F-453D-BE3A-24017A7158B8Q33926267-B26FE1FB-CEA2-4488-B13C-AFFDD5779112Q33939698-4F93D96D-F5B4-4E5E-B51A-0D8B8FEB07DBQ33959694-3EB070A3-5DC4-47D7-A3A6-BC60E31D80B5Q34375601-C38355FF-CA03-429E-9658-82147718BF9BQ34491255-9AA796E9-65BB-4677-A98E-016458B86B4AQ35220268-57FB5AB4-F161-4A29-BB05-DB465AA1EE49Q35783192-01C3716B-6EB1-48E6-A299-7A2BA52A7425Q35910595-15FB99FD-F5A8-4D98-AE76-DFCB6987F50CQ36150684-8A5CE25C-26E8-4BE1-8F11-775BD1C88C12Q36369721-81328F6C-192F-4E8A-90AE-DD20E1FEA372Q36389877-06FB048F-A281-4F0F-9D63-EC2960AAD52DQ36515529-2E0F870C-354F-4255-9AB9-A21F2B155657Q37094143-CD97339B-3E27-4158-BC7E-5702278E2703Q37137880-8C44CF47-64DC-47A3-906A-60FFA3B82ED8Q37297694-AF3CBA50-644D-424F-A275-7A97FD2211ACQ37602385-41740182-C6C4-4AD2-90E6-48D887F2E879Q37709774-4910C1F5-EAAB-4A1F-A432-16FECFBAB58FQ38280811-588CBE6F-90E4-47F0-A655-C4339C1CF4B3Q38372097-6E8E6EE7-BE74-4456-AB11-A7AD61C57231Q38427027-182A4BC1-E5B1-4351-BA57-7D04A305595FQ38616267-D550357A-FB48-4279-A468-1CAFE36C2948Q40067843-9C98A271-41D5-4474-A9CE-598143E71112Q40465920-49509EE9-3EDA-422C-BF03-512B7A22E2F6Q41900685-ABD0CD1A-09A3-4E4A-9C98-A63F111947A4Q42009973-96026C29-BC2B-4C5F-B988-EF5FAD4E2551Q42070241-EF324D6B-95B4-4A1B-803D-F65F41DD273AQ42291151-816AEB41-A663-434A-B9FE-49AE5EE26F5CQ42673943-E11DD650-380C-41CF-97F6-3E2B0DE73C55Q42692866-3C1B82BF-787F-4E0A-94D4-D2A075F3AC54Q42776369-4C423416-4153-436A-8645-F5298995FC21
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-1409-3095
@en
name
William Greenleaf
@ast
William Greenleaf
@en
William Greenleaf
@es
William Greenleaf
@nl
type
label
William Greenleaf
@ast
William Greenleaf
@en
William Greenleaf
@es
William Greenleaf
@nl
prefLabel
William Greenleaf
@ast
William Greenleaf
@en
William Greenleaf
@es
William Greenleaf
@nl
P214
P244
P106
P214
P244
no2012110568
P31
P496
0000-0003-1409-3095
P734
P7859
lccn-no2012110568