Detalhe da pesquisa
1.
StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants.
Am J Hum Genet
; 109(2): 195-209, 2022 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35032432
2.
Opportunities and challenges for the computational interpretation of rare variation in clinically important genes.
Am J Hum Genet
; 108(4): 535-548, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33798442
3.
Phylogenomics of the extinct Heath Hen provides support for sex-biased introgression among extant prairie grouse.
Mol Phylogenet Evol
; 189: 107927, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37714443
4.
Vibrio cholerae biofilm growth program and architecture revealed by single-cell live imaging.
Proc Natl Acad Sci U S A
; 113(36): E5337-43, 2016 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27555592
5.
ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden.
Genome Med
; 15(1): 51, 2023 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37443081
6.
Application of full-genome analysis to diagnose rare monogenic disorders.
NPJ Genom Med
; 6(1): 77, 2021 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34556655
7.
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders.
NPJ Genom Med
; 6(1): 88, 2021 Oct 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34642307