Harriet Dashnow
Harriet Dashnow
Geverifieerd e-mailadres voor genetics.utah.edu - Homepage
Titel
Geciteerd door
Geciteerd door
Jaar
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), 1-16, 2014
6852014
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
672018
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), 1-10, 2015
65*2015
Ten simple rules for writing a PLOS ten simple rules article
H Dashnow, A Lonsdale, PE Bourne
PLoS computational biology 10 (10), e1003858, 2014
172014
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
122017
Elegant SciPy: The art of scientific python
J Nunez-Iglesias, S Van Der Walt, H Dashnow
" O'Reilly Media, Inc.", 2017
92017
Genotyping microsatellites in next-generation sequencing data
H Dashnow, S Tan, D Das, S Easteal, A Oshlack
Bmc Bioinformatics 16 (2), 1-2, 2015
82015
Ten simple rules for a bioinformatics journal club
A Lonsdale, J Sietsma Penington, T Rice, M Walker, H Dashnow
PLoS computational biology 12 (1), e1004526, 2016
72016
SRST2: Rapid genomic surveillance for public health and hospital microbiology labs. Genome Med., 6
M Inouye, H Dashnow, LA Raven, MB Schultz, BJ Pope, T Tomita, J Zobel, ...
Epub ahead of print, 2014
62014
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
Public Library of Science 7 (9), e44974, 2012
62012
Effective variant filtering and expected candidate variant yield in studies of rare human disease
BS Pedersen, JM Brown, H Dashnow, AD Wallace, M Velinder, ...
NPJ Genomic Medicine 6 (1), 1-8, 2021
32021
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
22019
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
12019
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
Bioinformatics methods and approaches to discover disease variants from DNA sequencing data
H Dashnow
2019
Comparing algorithms to genotype short tandem repeats in next-generation sequencing data
H Dashnow, A Oshlack
F1000Research 4, 2015
2015
1: RNA-Seq reads to counts
MDM Doyle, B Phipson, H Dashnow, QC Understand, RB Uploader
2: RNA-seq counts to genes
MDM Doyle, B Phipson, J Maksimovic, A Trigos, M Ritchie, H Dashnow, ...
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–18