Detalhe da pesquisa
1.
Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs.
Cell
; 183(1): 197-210.e32, 2020 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33007263
2.
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Nature
; 590(7845): 290-299, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33568819
3.
Diverse tumorigenic consequences of human papillomavirus integration in primary oropharyngeal cancers.
Genome Res
; 32(1): 55-70, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34903527
4.
Human papillomavirus and the landscape of secondary genetic alterations in oral cancers.
Genome Res
; 29(1): 1-17, 2019 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30563911
5.
Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations.
BMC Genomics
; 22(1): 666, 2021 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34719381
6.
Gustaf: Detecting and correctly classifying SVs in the NGS twilight zone.
Bioinformatics
; 30(24): 3484-90, 2014 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25028727
7.
The gout epidemic in French Polynesia: a modelling study of data from the Ma'i u'u epidemiological survey.
Lancet Glob Health
; 12(4): e685-e696, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38485432
8.
Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads.
Bioinformatics
; 28(7): 1024-5, 2012 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-22302574
9.
Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS.
Bioinformatics
; 28(5): 619-27, 2012 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-22238266
10.
RazerS--fast read mapping with sensitivity control.
Genome Res
; 19(9): 1646-54, 2009 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-19592482
11.
Somatic whole genome dynamics of precancer in Barrett's esophagus reveals features associated with disease progression.
Nat Commun
; 13(1): 2300, 2022 04 28.
Artigo
Inglês
| MEDLINE | ID: mdl-35484108
12.
A novel and well-defined benchmarking method for second generation read mapping.
BMC Bioinformatics
; 12: 210, 2011 May 26.
Artigo
Inglês
| MEDLINE | ID: mdl-21615913
13.
MicroRazerS: rapid alignment of small RNA reads.
Bioinformatics
; 26(1): 123-4, 2010 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-19880369
14.
A consistency-based consensus algorithm for de novo and reference-guided sequence assembly of short reads.
Bioinformatics
; 25(9): 1118-24, 2009 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-19269990
15.
Author Correction: PGBD5 promotes site-specific oncogenic mutations in human tumors.
Nat Genet
; 52(11): 1265, 2020 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-32918070
16.
Segment-based multiple sequence alignment.
Bioinformatics
; 24(16): i187-92, 2008 Aug 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18689823
17.
Genetic mechanisms of primary chemotherapy resistance in pediatric acute myeloid leukemia.
Leukemia
; 33(8): 1934-1943, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-30760869
18.
Sequencing and curation strategies for identifying candidate glioblastoma treatments.
BMC Med Genomics
; 12(1): 56, 2019 04 25.
Artigo
Inglês
| MEDLINE | ID: mdl-31023376
19.
Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments.
BMC Med Genomics
; 12(1): 114, 2019 Aug 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31375115
20.
Genome-wide somatic variant calling using localized colored de Bruijn graphs.
Commun Biol
; 1: 20, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-30271907