Detalhe da pesquisa
1.
Characterization of telomere variant repeats using long reads enables allele-specific telomere length estimation.
BMC Bioinformatics
; 25(1): 194, 2024 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38755561
2.
Activation of homology-directed DNA repair plays key role in CRISPR-mediated genome correction.
Gene Ther
; 30(3-4): 386-397, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36258038
3.
Telogator: a method for reporting chromosome-specific telomere lengths from long reads.
Bioinformatics
; 38(7): 1788-1793, 2022 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35022670
4.
CpGtools: a python package for DNA methylation analysis.
Bioinformatics
; 37(11): 1598-1599, 2021 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31808791
5.
Recurrent MSC E116K mutations in ALK-negative anaplastic large cell lymphoma.
Blood
; 133(26): 2776-2789, 2019 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31101622
6.
Ccne1 Overexpression Causes Chromosome Instability in Liver Cells and Liver Tumor Development in Mice.
Gastroenterology
; 157(1): 210-226.e12, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30878468
7.
Combining copy number, methylation markers, and mutations as a panel for endometrial cancer detection via intravaginal tampon collection.
Gynecol Oncol
; 156(2): 387-392, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31787246
8.
Indel detection from RNA-seq data: tool evaluation and strategies for accurate detection of actionable mutations.
Brief Bioinform
; 18(6): 973-983, 2017 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27473065
9.
Linnorm: improved statistical analysis for single cell RNA-seq expression data.
Nucleic Acids Res
; 45(22): e179, 2017 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28981748
10.
Exploring genetic associations with ceRNA regulation in the human genome.
Nucleic Acids Res
; 45(10): 5653-5665, 2017 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28472449
11.
mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers.
Nucleic Acids Res
; 45(W1): W215-W221, 2017 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28482068
12.
Novel Neural Network Approach to Predict Drug-Target Interactions Based on Drug Side Effects and Genome-Wide Association Studies.
Hum Hered
; 83(2): 79-91, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30347404
13.
Detection and visualization of complex structural variants from long reads.
BMC Bioinformatics
; 19(Suppl 20): 508, 2018 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30577744
14.
HGT-ID: an efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data.
BMC Bioinformatics
; 19(1): 271, 2018 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30016933
15.
A data science approach for the classification of low-grade and high-grade ovarian serous carcinomas.
BMC Genomics
; 19(1): 841, 2018 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30482155
16.
Early genetic aberrations in patients with sporadic colorectal cancer.
Mol Carcinog
; 57(1): 114-124, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28926134
17.
VCF-Miner: GUI-based application for mining variants and annotations stored in VCF files.
Brief Bioinform
; 17(2): 346-51, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26210358
18.
Correction to: the impact of pharmacokinetic gene profiles across human cancers.
BMC Cancer
; 18(1): 743, 2018 07 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30021563
19.
The impact of pharmacokinetic gene profiles across human cancers.
BMC Cancer
; 18(1): 577, 2018 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29783934
20.
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.
Nucleic Acids Res
; 44(D1): D869-76, 2016 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26615194