Follow
Harriet Dashnow
Harriet Dashnow
Verified email at genetics.utah.edu - Homepage
Title
Cited by
Cited by
Year
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, 1-16, 2014
1057*2014
STRetch: detecting and discovering pathogenic short tandem repeat expansions
H Dashnow, M Lek, B Phipson, A Halman, S Sadedin, A Lonsdale, ...
Genome biology 19, 1-13, 2018
1392018
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, 1-10, 2015
1022015
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), 60, 2021
692021
Characterization and visualization of tandem repeats at genome scale
E Dolzhenko, A English, H Dashnow, G De Sena Brandine, T Mokveld, ...
Nature Biotechnology, 1-9, 2024
38*2024
STRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel loci
H Dashnow, BS Pedersen, L Hiatt, J Brown, SJ Beecroft, G Ravenscroft, ...
Genome Biology 23 (1), 257, 2022
322022
Elegant SciPy: The Art of Scientific Python
J Nunez-Iglesias, S Van der Walt, H Dashnow
" O'Reilly Media, Inc.", 2017
322017
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
272017
Ten simple rules for writing a PLOS ten simple rules article
H Dashnow, A Lonsdale, PE Bourne
PLoS Computational Biology 10 (10), e1003858, 2014
262014
Sequencing and characterizing short tandem repeats in the human genome
HA Tanudisastro, IW Deveson, H Dashnow, DG MacArthur
Nature Reviews Genetics, 1-16, 2024
212024
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
172019
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation
JA Gustafson, SB Gibson, N Damaraju, MPG Zalusky, K Hoekzema, ...
medRxiv, 2024
122024
Genotyping microsatellites in next-generation sequencing data
H Dashnow, S Tan, D Das, S Easteal, A Oshlack
Bmc Bioinformatics 16 (Suppl 2), A5, 2015
122015
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
112016
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
92012
Chronic Lactation Insufficiency Is a Public Health Issue: Commentary on “We Need Patient-Centered Research in Breastfeeding Medicine” by Stuebe. Breastfeed Med 2021; 16: 349–350.
H Shere, L Weijer, H Dashnow, LE Moreno, S Foxworthy Scott, H Baker
Breastfeeding Medicine 16 (12), 933-934, 2021
82021
A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigree
D Porubsky, H Dashnow, TA Sasani, GA Logsdon, P Hallast, MD Noyes, ...
bioRxiv, 2024
42024
RNA‐seq analysis in R
B Phipson, A Trigos, M Ritchie, S Su, M Doyle, H Dashnow, C Law
32020
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
32019
1: RNA-Seq reads to counts
M Doyle, B Phipson, H Dashnow
Galaxy Training Network, 2019
3*2019
The system can't perform the operation now. Try again later.
Articles 1–20