Harriet Dashnow
Harriet Dashnow
Verified email at genetics.utah.edu - Homepage
TitleCited byYear
SRST2: rapid genomic surveillance for public health and hospital microbiology labs
M Inouye, H Dashnow, LA Raven, MB Schultz, BJ Pope, T Tomita, J Zobel, ...
Genome medicine 6 (11), 90, 2014
4572014
Cpipe: a shared variant detection pipeline designed for diagnostic settings
SP Sadedin, H Dashnow, PA James, M Bahlo, DC Bauer, A Lonie, ...
Genome medicine 7 (1), 68, 2015
45*2015
STRetch: detecting and discovering pathogenic short tandem repeat expansions
H Dashnow, M Lek, B Phipson, A Halman, S Sadedin, A Lonsdale, ...
Genome biology 19 (1), 1-13, 2018
272018
A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data
Z Stark, H Dashnow, S Lunke, TY Tan, A Yeung, S Sadedin, N Thorne, ...
European Journal of Human Genetics 25 (11), 1268-1272, 2017
112017
Ten simple rules for writing a PLOS ten simple rules article
H Dashnow, A Lonsdale, PE Bourne
PLoS computational biology 10 (10), 2014
112014
Elegant SciPy: The Art of Scientific Python
J Nunez-Iglesias, S Van Der Walt, S Walt, H Dashnow
" O'Reilly Media, Inc.", 2017
52017
Development of transgenic mice containing an introduced stop codon on the human methylmalonyl-CoA mutase locus
NE Buck, H Dashnow, JJ Pitt, LR Wood, HL Peters
PloS one 7 (9), 2012
52012
Ten simple rules for a bioinformatics journal club
A Lonsdale, JS Penington, T Rice, M Walker, H Dashnow
PLoS computational biology 12 (1), 2016
42016
Genotyping microsatellites in next-generation sequencing data
H Dashnow, S Tan, D Das, S Easteal, A Oshlack
BMC bioinformatics 16 (2), A5, 2015
42015
Data Interlocking: Coupling analytics to the data
Y Kowsar, H Dashnow, A Lonie
2014 IEEE/ACM 7th International Conference on Utility and Cloud Computing …, 2014
12014
Bionitio: demonstrating and facilitating best practices for bioinformatics command-line software
P Georgeson, A Syme, C Sloggett, J Chung, H Dashnow, M Milton, ...
GigaScience 8 (9), giz109, 2019
2019
Bioinformatics methods and approaches to discover disease variants from DNA sequencing data
H Dashnow
2019
Pooled-parent exome sequencing to prioritise de novo variants in genetic disease
H Dashnow, KM Bell, Z Stark, TY Tan, SM White, A Oshlack
BioRxiv, 601740, 2019
2019
Comparing algorithms to genotype short tandem repeats in next-generation sequencing data
H Dashnow, A Oshlack
F1000Research 4, 2015
2015
RNA-seq analysis in R
B Phipson, M Doyle, H Dashnow
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Articles 1–15