# HG changeset patch
# User yhoogstrate
# Date 1427301465 14400
# Node ID ac69be28e78697c72b58f97d201716bc1de5ba0b
# Parent ab3ea877607f8bc815f6ebe69a8451c371599fdc
FlaiMapper: added wrapper for FASTA->GTF conversion
diff -r ab3ea877607f -r ac69be28e786 flaimapper-gtf-from-fasta.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/flaimapper-gtf-from-fasta.xml Wed Mar 25 12:37:45 2015 -0400
@@ -0,0 +1,98 @@
+
+
+ Extract GTF file from FASTA file (as FlaiMapper reference).
+
+ pysam
+ flaimapper
+
+
+ flaimapper --version
+
+
+ gtf-from-fasta
+ -o $output
+ $fasta
+
+
+
+
+
+
+
+
+
+
+
+FlaiMapper wrapper for Galaxy
+=============================
+
+https://github.com/yhoogstrate/flaimapper
+http://www.ncbi.nlm.nih.gov/pubmed/25338717
+http://dx.doi.org/10.1093/bioinformatics/btu696
+
+Fragment Location Annotation Identification Mapper
+
+FlaiMapper: computational annotation of small ncRNA-derived fragments using RNA-seq high-throughput data.
+
+Input formats
+-------------
+To make FlaiMapper compatible with both an entire reference genome as a
+separate ncRNA database, it requires an additional GTF file *(mask file)*.
+The major difference between an entire reference and a ncRNA database
+is that an entire reference usually contains multiple ncRNAs per sequence
+entry (chromosome). While for the ncRNA database, each entry should
+represent one single mature ncRNA.
+
+Therefore the mask file that represents to the FASTA file of a ncRNA
+database will only contain the start- and end positions of each entry.
+To generate this in an automated fashion, you can make use of this tool
+*as long as the FASTA file doesn't contain entire chromosomes* but
+mature ncRNA.
+
+An example input file is **ncRNAdb09**, available at the following URLs:
+https://raw.githubusercontent.com/yhoogstrate/flaimapper/master/share/annotations/ncRNA_annotation/ncrnadb09.fa *(reference file)*
+
+It should generate a GTF/GFF file (mask file) similar to the following URL:
+https://raw.githubusercontent.com/yhoogstrate/flaimapper/master/share/annotations/ncRNA_annotation/ncrnadb09.gtf *(mask file)*
+
+Installation
+------------
+
+The wrapper makes use of easy_install to install a python egg. Please
+ensure you have easy_install installed.
+
+License
+-------
+
+**flaimapper** and **wrapper**:
+
+GPL (>=3)
+
+**pysam**:
+
+The MIT License
+
+Contact
+-------
+
+The tool wrapper has been written by Youri Hoogstrate from the Erasmus
+Medical Center (Rotterdam, Netherlands).
+
+
+Development
+-----------
+
+* Repository-Maintainer: Youri Hoogstrate
+* Repository-Developers: Youri Hoogstrate
+
+* Repository-Development: https://bitbucket.org/EMCbioinf/galaxy-tool-shed-tools
+
+The tool wrapper has been written by Youri Hoogstrate from the Erasmus
+Medical Center (Rotterdam, Netherlands).
+
+
+
+
+ 10.1093/bioinformatics/btu696
+
+
diff -r ab3ea877607f -r ac69be28e786 flaimapper.xml
--- a/flaimapper.xml Fri Mar 20 11:14:32 2015 -0400
+++ b/flaimapper.xml Wed Mar 25 12:37:45 2015 -0400
@@ -60,7 +60,7 @@
- http://genome.ucsc.edu/FAQ/FAQformat.html#format3
- http://www.ensembl.org/info/website/upload/gff.html
-The reference sequence should be provided in FASTSA format.
+The reference sequence should be provided in FASTA format.
You can access **ncRNAdb09** at the following URLs:
https://raw.githubusercontent.com/yhoogstrate/flaimapper/master/share/annotations/ncRNA_annotation/ncrnadb09.gtf *(mask file)*
@@ -112,19 +112,9 @@
The tool wrapper has been written by Youri Hoogstrate from the Erasmus
Medical Center (Rotterdam, Netherlands).
-References
-----------
-**FlaiMapper: computational annotation of small ncRNA-derived fragments using RNA-seq high-throughput data.**
-
-*Hoogstrat* - Bioinformatics. 2014 Apr 1;30(7):923-30.
-
-*Youri Hoogstrate, Guido Jenster, and Elena S. Martens-Uzunova* - Bioinformatics (2015) 31 (5): 665-673
-
-- http://www.ncbi.nlm.nih.gov/pubmed/25338717
-- http://dx.doi.org/10.1093/bioinformatics/btu696
10.1093/bioinformatics/btu696
-
\ No newline at end of file
+