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ADGC Publications
Found 6 results
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Sequence Analysis, DNA
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2018
Nafikov RA
,
Nato AQ
,
Sohi H
,
Wang B
,
Brown L
,
Horimoto AR
,
Vardarajan BN
,
Barral SM
,
Tosto G
,
Mayeux RP
et al.
. 2018.
Analysis of Pedigree Data in Populations with Multiple Ancestries: Strategies for Dealing with Admixture in Caribbean Hispanic Families from the ADSP.
.
Genet Epidemiol. 42(6):500-515.
Blue EE
,
Bis JC
,
Dorschner MO
,
Tsuang DW
,
Barral SM
,
Beecham G
,
Below JE
,
Bush WS
,
Butkiewicz M
,
Cruchaga C
et al.
. 2018.
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
.
Dement Geriatr Cogn Disord. 45(1-2):1-17.
2017
Butkiewicz M
,
Haines JL
,
Bush WS
. 2017.
Introducing COCOS: codon consequence scanner for annotating reading frame changes induced by stop-lost and frame shift variants.
.
Bioinformatics. 33(10):1561-1562.
2015
Nho K
,
Kim S
,
Risacher SL
,
Shen L
,
Corneveaux JJ
,
Swaminathan S
,
Lin H
,
Ramanan VK
,
Liu Y
,
Foroud TM
et al.
. 2015.
Protective variant for hippocampal atrophy identified by whole exome sequencing.
.
Ann Neurol. 77(3):547-52.
2013
Lin C-F
,
Valladares O
,
D Childress M
,
Klevak E
,
Geller ET
,
Hwang, ii Y-C
,
Tsai EA
,
Schellenberg GD
,
Wang L-S
. 2013.
DRAW+SneakPeek: analysis workflow and quality metric management for DNA-seq experiments.
.
Bioinformatics. 29(19):2498-500.
Schafer CM
,
Campbell NG
,
Cai G
,
Yu F
,
Makarov V
,
Yoon S
,
Daly MJ
,
Gibbs RA
,
Schellenberg GD
,
Devlin B
et al.
. 2013.
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.
.
Genomics. 102(4):270-7.