-
Notifications
You must be signed in to change notification settings - Fork 0
/
Copy pathDESCRIPTION
29 lines (29 loc) · 1.1 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
29
Package: CNVcExp
Title: CNVcorrelatedExp
Version: 0.0.0.9000
Authors@R: c(
person(given = "Bruno-Rodrigo Assuncao", role = c("aut", "cre"), email = "[email protected]"),
person(given = "Lucas Brandao", role = c("ctb"),email = "[email protected]"),
person(given = "Ronald Moura", role = c("ctb"),email = "[email protected]"),
))
Description: Complete workflow to obtain a full Copy Number Variations Anotations Upon Genomic Abnormalities of Acute Myeloid Leukemia
for genomic or exomic sequence data. This operates the identification of Copy Number Variations, annotations of this variants, correlations to genetic expression and Classifie the leukemic subtipes througt molecular patherns..
License: `use_mit_license()`, `use_gpl3_license()` or friends to pick a
license
Encoding: UTF-8
Roxygen: list(markdown = TRUE)
RoxygenNote: 7.2.3
Author: Bruno-Rodrigo Assuncao [aut, cre],
Lucas Brandao [ctb],
Ronald Moura [ctb],
Sergio Crovela [ctb]
Imports:
cn.mops
GenomicFeatures
RMariaDB
org.Hs.eg.db
GenomicRanges
org.Hs.eg.db
biomaRt
doParallel
importFrom(foreach,"%dopar%")