Detalhe da pesquisa
1.
Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin.
Cell
; 158(4): 929-944, 2014 Aug 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-25109877
2.
Characterization and mitigation of artifacts derived from NGS library preparation due to structure-specific sequences in the human genome.
BMC Genomics
; 25(1): 227, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38429743
3.
OncoPubMiner: a platform for mining oncology publications.
Brief Bioinform
; 23(5)2022 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36058206
4.
RabbitQCPlus 2.0: More efficient and versatile quality control for sequencing data.
Methods
; 216: 39-50, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37330158
5.
A comprehensive performance evaluation, comparison, and integration of computational methods for detecting and estimating cross-contamination of human samples in cancer next-generation sequencing analysis.
J Biomed Inform
; 152: 104625, 2024 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38479675
6.
Comprehensive fundamental somatic variant calling and quality management strategies for human cancer genomes.
Brief Bioinform
; 22(3)2021 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32510555
7.
Comprehensive review and evaluation of computational methods for identifying FLT3-internal tandem duplication in acute myeloid leukaemia.
Brief Bioinform
; 22(5)2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33851200
8.
MSIsensor-ct: microsatellite instability detection using cfDNA sequencing data.
Brief Bioinform
; 22(5)2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33461213
9.
Identification of MKI67, TPR , and TCHH Mutations as Prognostic Biomarkers for Patients With Defective Mismatch Repair Colon Cancer Stage II/III.
Dis Colon Rectum
; 66(11): 1481-1491, 2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37643197
10.
RabbitQC: high-speed scalable quality control for sequencing data.
Bioinformatics
; 37(4): 573-574, 2021 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32790850
11.
HotSpot3D web server: an integrated resource for mutation analysis in protein 3D structures.
Bioinformatics
; 36(12): 3944-3946, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32315389
12.
GenomeVIP: a cloud platform for genomic variant discovery and interpretation.
Genome Res
; 27(8): 1450-1459, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28522612
13.
Mutational landscape and significance across 12 major cancer types.
Nature
; 502(7471): 333-339, 2013 Oct 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-24132290
14.
MetaSpark: a spark-based distributed processing tool to recruit metagenomic reads to reference genomes.
Bioinformatics
; 33(7): 1090-1092, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28065898
15.
MSIsensor: microsatellite instability detection using paired tumor-normal sequence data.
Bioinformatics
; 30(7): 1015-6, 2014 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24371154
16.
Ultrafast clustering algorithms for metagenomic sequence analysis.
Brief Bioinform
; 13(6): 656-68, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22772836
17.
MGAviewer: a desktop visualization tool for analysis of metagenomics alignment data.
Bioinformatics
; 29(1): 122-3, 2013 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23044549
18.
CD-HIT: accelerated for clustering the next-generation sequencing data.
Bioinformatics
; 28(23): 3150-2, 2012 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23060610
19.
Case Report: SMARCA4 (BRG1)-deficient undifferentiated carcinoma of gallbladder with genetic analysis.
Front Oncol
; 13: 1086266, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37456262
20.
Long-term response to camrelizumab in a pretreated metastatic mixed testicular germ-cell tumor patient with co-mutations in DNA damage-repair genes.
Immunotherapy
; 15(1): 17-25, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36647794