Detalhe da pesquisa
1.
Sources of erroneous sequences and artifact chimeric reads in next generation sequencing of genomic DNA from formalin-fixed paraffin-embedded samples.
Nucleic Acids Res
; 47(2): e12, 2019 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30418619
2.
RNA-Seq Analysis of Gene Expression, Viral Pathogen, and B-Cell/T-Cell Receptor Signatures in Complex Chronic Disease.
Clin Infect Dis
; 64(4): 476-481, 2017 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28172519
3.
Increasing quality, throughput and speed of sample preparation for strand-specific messenger RNA sequencing.
BMC Genomics
; 18(1): 515, 2017 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28679365
4.
Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma.
Nature
; 476(7360): 298-303, 2011 Jul 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-21796119
5.
Functional genomics of the cilium, a sensory organelle.
Curr Biol
; 15(10): 935-41, 2005 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-15916950
6.
Automated high throughput nucleic acid purification from formalin-fixed paraffin-embedded tissue samples for next generation sequence analysis.
PLoS One
; 12(6): e0178706, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28570594
7.
Improved resolution of phenotypic subsets in human T-ALL by incorporation of RNA-seq based developmental profiling.
Leuk Res
; 110: 106712, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34583126
8.
Surveillance of the tumor mutanome by T cells during progression from primary to recurrent ovarian cancer.
Clin Cancer Res
; 20(5): 1125-34, 2014 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24323902
9.
A clinically validated diagnostic second-generation sequencing assay for detection of hereditary BRCA1 and BRCA2 mutations.
J Mol Diagn
; 15(6): 796-809, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24094589