Detalhe da pesquisa
1.
Ordered and deterministic cancer genome evolution after p53 loss.
Nature
; 608(7924): 795-802, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35978189
2.
A RSC/nucleosome complex determines chromatin architecture and facilitates activator binding.
Cell
; 141(3): 407-18, 2010 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-20434983
3.
Copolymerization of single-cell nucleic acids into balls of acrylamide gel.
Genome Res
; 30(1): 49-61, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31727682
4.
Multiplex accurate sensitive quantitation (MASQ) with application to minimal residual disease in acute myeloid leukemia.
Nucleic Acids Res
; 48(7): e40, 2020 04 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32083660
5.
Role of SWI/SNF in acute leukemia maintenance and enhancer-mediated Myc regulation.
Genes Dev
; 27(24): 2648-62, 2013 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24285714
6.
The contribution of de novo coding mutations to autism spectrum disorder.
Nature
; 515(7526): 216-21, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363768
7.
SMASH, a fragmentation and sequencing method for genomic copy number analysis.
Genome Res
; 26(6): 844-51, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27197213
8.
Optimizing sparse sequencing of single cells for highly multiplex copy number profiling.
Genome Res
; 25(5): 714-24, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25858951
9.
Interactive analysis and assessment of single-cell copy-number variations.
Nat Methods
; 12(11): 1058-60, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26344043
10.
Tumour evolution inferred by single-cell sequencing.
Nature
; 472(7341): 90-4, 2011 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21399628
11.
The maize methylome influences mRNA splice sites and reveals widespread paramutation-like switches guided by small RNA.
Genome Res
; 23(10): 1651-62, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23739895
12.
Rare de novo germline copy-number variation in testicular cancer.
Am J Hum Genet
; 91(2): 379-83, 2012 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22863192
13.
Limited genomic heterogeneity of circulating melanoma cells in advanced stage patients.
Phys Biol
; 12(1): 016008, 2015 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25574741
14.
Reducing system noise in copy number data using principal components of self-self hybridizations.
Proc Natl Acad Sci U S A
; 109(3): E103-10, 2012 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22207624
15.
The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
Hum Genet
; 133(1): 11-27, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23979609
16.
Magnetically functionalized hydrogels for high-throughput genomic applications.
Adv Mater Technol
; 9(2)2024 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38645306
17.
Inferring tumor progression from genomic heterogeneity.
Genome Res
; 20(1): 68-80, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19903760
18.
FABP5 Inhibition against PTEN-Mutant Therapy Resistant Prostate Cancer.
Cancers (Basel)
; 16(1)2023 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38201488
19.
High definition profiling of mammalian DNA methylation by array capture and single molecule bisulfite sequencing.
Genome Res
; 19(9): 1593-605, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19581485
20.
Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA).
Blood
; 113(6): 1294-303, 2009 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18922857