-
Notifications
You must be signed in to change notification settings - Fork 2
/
Copy pathDESCRIPTION
28 lines (28 loc) · 1.05 KB
/
DESCRIPTION
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
Package: highlineR
Title: A Novel Visualization Tool to Assess Diversity in NGS Data
Version: 0.1
Authors@R: c(person("Lisa-Monique", "Edward", email = "[email protected]", role = c("aut")),
person("Art", "Poon", email = "[email protected]", role = "cre"))
Description: A novel visualization tool to assess diversity in NGS data. Similar to the Los
Alamos Highlighter tool, highlineR highlights mismatches, transition and
transversion mutations, and synonymous and non-synonymous mutations in aligned
protein or nucleotide sequences. This tool also visualizes the relative
frequency of sequence variants and is particularly useful for visualizing
sequence diversity, potential recombination and super-infection.
Depends: R (>= 3.5)
License: GPL-3
Encoding: UTF-8
LazyData: true
Imports:
ggplot2 (>= 3.1.1),
ggpubr (>= 0.2),
utils
Suggests:
ape (>= 5.3),
parallel (>= 3.5.1),
knitr,
rmarkdown,
testthat (>= 2.0.1),
BugReports: https://github.com/poonlab/highlineR/issues
RoxygenNote: 6.1.1
VignetteBuilder: knitr