Detalhe da pesquisa
1.
Genetic drivers and cellular selection of female mosaic X chromosome loss.
Nature
; 2024 Jun 12.
Artigo
Inglês
| MEDLINE | ID: mdl-38867047
2.
KATK: Fast genotyping of rare variants directly from unmapped sequencing reads.
Hum Mutat
; 42(6): 777-786, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33715282
3.
GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads.
Sci Rep
; 13(1): 17765, 2023 10 18.
Artigo
Inglês
| MEDLINE | ID: mdl-37853040
4.
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events.
medRxiv
; 2023 Nov 27.
Artigo
Inglês
| MEDLINE | ID: mdl-38076931
5.
Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection.
medRxiv
; 2023 Jan 31.
Artigo
Inglês
| MEDLINE | ID: mdl-36778285
6.
AluMine: alignment-free method for the discovery of polymorphic Alu element insertions.
Mob DNA
; 10: 31, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31360240
7.
FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads.
Sci Rep
; 7(1): 2537, 2017 05 31.
Artigo
Inglês
| MEDLINE | ID: mdl-28566690