Detalhe da pesquisa
1.
Explicable prioritization of genetic variants by integration of rule-based and machine learning algorithms for diagnosis of rare Mendelian disorders.
Hum Genomics
; 18(1): 28, 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38509596
2.
Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia.
Am J Hum Genet
; 104(3): 439-453, 2019 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30773278
3.
3Cnet: pathogenicity prediction of human variants using multitask learning with evolutionary constraints.
Bioinformatics
; 37(24): 4626-4634, 2021 12 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34270679
4.
Utilizing random Forest QSAR models with optimized parameters for target identification and its application to target-fishing server.
BMC Bioinformatics
; 18(Suppl 16): 567, 2017 12 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-29297315
5.
Case Report: Infantile Cerebellar-Retinal Degeneration With Compound Heterozygous Variants in ACO2 Gene-Long-Term Follow-Up of a Sibling.
Front Genet
; 13: 729980, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35368710
6.
In-Silico Molecular Binding Prediction for Human Drug Targets Using Deep Neural Multi-Task Learning.
Genes (Basel)
; 10(11)2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31703452
7.
Using reverse docking for target identification and its applications for drug discovery.
Expert Opin Drug Discov
; 11(7): 707-15, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27186904