Detalhe da pesquisa
1.
Ancestry-agnostic estimation of DNA sample contamination from sequence reads.
Genome Res
; 30(2): 185-194, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31980570
2.
LocusZoom.js: interactive and embeddable visualization of genetic association study results.
Bioinformatics
; 37(18): 3017-3018, 2021 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33734315
3.
Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data.
Am J Hum Genet
; 97(2): 284-90, 2015 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26235984
4.
Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data.
Am J Hum Genet
; 91(5): 839-48, 2012 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23103226
5.
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.
Proc Natl Acad Sci U S A
; 106(18): 7501-6, 2009 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19416921
6.
Developing and deploying an integrated workshop curriculum teaching computational skills for reproducible research.
J Open Source Educ
; 5(47)2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35224460
7.
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.
Nat Commun
; 9(1): 3753, 2018 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30218074
8.
Exome Sequencing of Familial Bipolar Disorder.
JAMA Psychiatry
; 73(6): 590-7, 2016 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27120077
9.
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes.
Psychophysiology
; 51(12): 1309-20, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25387710