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Sequence Analysis, DNA
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2020
Wheeler NR
,
Benchek P
,
Kunkle BW
,
Hamilton-Nelson KL
,
Warfe M
,
Fondran JR
,
Haines JL
,
Bush WS
. 2020.
Hadoop and PySpark for reproducibility and scalability of genomic sequencing studies.
.
Pac Symp Biocomput. 25:523-534.
PubMed
2019
Saad M
,
Wijsman EM
. 2019.
Association score testing for rare variants and binary traits in family data with shared controls.
.
Brief Bioinform. 20(1):245-253.
PubMed
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.
PubMed
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.
PubMed
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.
PubMed
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