Artículos con órdenes de acceso público - Deanna ChurchMás información
No disponible en ningún lugar: 1
A next-generation human genome sequence
DM Church
Science 376 (6588), 34-35, 2022
Órdenes: European Commission
Disponibles en algún lugar: 39
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Órdenes: US National Institutes of Health, Howard Hughes Medical Institute, British …
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Management Group Liefer Laura A. 51 Wetterstrand Kris A. 51 Good Peter J. 51 ...
nature 447 (7146), 799-816, 2007
Órdenes: German Research Foundation
Database resources of the national center for biotechnology information
EW Sayers, T Barrett, DA Benson, E Bolton, SH Bryant, K Canese, ...
Nucleic acids research 39 (suppl_1), D38-D51, 2010
Órdenes: US National Institutes of Health
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
DT Miller, MP Adam, S Aradhya, LG Biesecker, AR Brothman, NP Carter, ...
The American Journal of Human Genetics 86 (5), 749-764, 2010
Órdenes: US National Institutes of Health, Howard Hughes Medical Institute
ClinVar: public archive of relationships among sequence variation and human phenotype
MJ Landrum, JM Lee, GR Riley, W Jang, WS Rubinstein, DM Church, ...
Nucleic acids research 42 (D1), D980-D985, 2014
Órdenes: US National Institutes of Health
Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly
VA Schneider, T Graves-Lindsay, K Howe, N Bouk, HC Chen, PA Kitts, ...
Genome research 27 (5), 849-864, 2017
Órdenes: US National Institutes of Health, Howard Hughes Medical Institute, European …
Direct determination of diploid genome sequences
NI Weisenfeld, V Kumar, P Shah, DM Church, DB Jaffe
Genome research 27 (5), 757-767, 2017
Órdenes: US National Institutes of Health
Multi-platform discovery of haplotype-resolved structural variation in human genomes
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Nature communications 10 (1), 1784, 2019
Órdenes: US National Institutes of Health, National Health and Medical Research …
Lineage-specific biology revealed by a finished genome assembly of the mouse
DM Church, L Goodstadt, LDW Hillier, MC Zody, S Goldstein, X She, ...
PLoS biology 7 (5), e1000112, 2009
Órdenes: Swiss National Science Foundation, US National Institutes of Health
Modernizing reference genome assemblies
DM Church, VA Schneider, T Graves, K Auger, F Cunningham, N Bouk, ...
PLoS biology 9 (7), e1001091, 2011
Órdenes: US National Institutes of Health, Howard Hughes Medical Institute
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
EB Kaminsky, V Kaul, J Paschall, DM Church, B Bunke, D Kunig, ...
Genetics in medicine 13 (9), 777-784, 2011
Órdenes: US National Institutes of Health
Assembly: a resource for assembled genomes at NCBI
PA Kitts, DM Church, F Thibaud-Nissen, J Choi, V Hem, V Sapojnikov, ...
Nucleic acids research 44 (D1), D73-D80, 2016
Órdenes: US National Institutes of Health
The emergent landscape of the mouse gut endoderm at single-cell resolution
S Nowotschin, M Setty, YY Kuo, V Liu, V Garg, R Sharma, CS Simon, ...
Nature 569 (7756), 361-367, 2019
Órdenes: US National Institutes of Health, Natural Sciences and Engineering Research …
DbVar and DGVa: public archives for genomic structural variation
I Lappalainen, J Lopez, L Skipper, T Hefferon, JD Spalding, J Garner, ...
Nucleic acids research 41 (D1), D936-D941, 2012
Órdenes: US National Institutes of Health
Mouse segmental duplication and copy number variation
X She, Z Cheng, S Zöllner, DM Church, EE Eichler
Nature genetics 40 (7), 909-914, 2008
Órdenes: US National Institutes of Health, Howard Hughes Medical Institute
Resolving the full spectrum of human genome variation using Linked-Reads
P Marks, S Garcia, AM Barrio, K Belhocine, J Bernate, R Bharadwaj, ...
Genome research 29 (4), 635-645, 2019
Órdenes: US National Institutes of Health
Dissecting the causal mechanism of X-linked dystonia-parkinsonism by integrating genome and transcriptome assembly
T Aneichyk, WT Hendriks, R Yadav, D Shin, D Gao, CA Vaine, RL Collins, ...
Cell 172 (5), 897-909. e21, 2018
Órdenes: US National Institutes of Health, Howard Hughes Medical Institute
A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing
AA Petti, SR Williams, CA Miller, IT Fiddes, SN Srivatsan, DY Chen, ...
Nature communications 10 (1), 3660, 2019
Órdenes: US National Institutes of Health
Extending reference assembly models
DM Church, VA Schneider, KM Steinberg, MC Schatz, AR Quinlan, ...
Genome biology 16, 1-5, 2015
Órdenes: US National Institutes of Health, European Molecular Biology Laboratory …
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