Référentiel des outils installés sur la plateforme Migale
La liste des packages R installés sur la plateforme Migale est disponible ici.
fasta (version 3.6 - 2014-02-21)
A set of sequence comparison tools (fasta36, ggsearch...) used for alignment and database searching.For example, fasta compares a protein sequence to another protein sequence or to a protein database, or a DNA sequence to another DNA sequence or a DNA library.
Documentation : http://fasta.bioch.virginia.edu/fasta_www2/fasta_intro.shtml
Usage : #fasta36
FastQC (version 0.10.0 - 2012-03-05)
FastQC aims to provide a simple way to do some quality control checks on raw sequence data coming from high throughput sequencing pipelines. It provides a modular set of analyses which you can use to give a quick impression of whether your data has any problems of which you should be aware before doing any further analysis.
Documentation : http://www.bioinformatics.bbsrc.ac.uk/projects/fastqc/Help/
Usage : #fastqc ou fastqc seqfile1 seqfile2 .. seqfileN
fastqp (version 0.1.9.1 - 2017-02-27)
Simple FASTQ, SAM and BAM read quality assessment and plotting using Python.
Download : https://github.com/mdshw5/fastqp
Documentation : https://github.com/mdshw5/fastqp
Usage : #fastqp [-h]
Fastq_Screen (version 0.4.4 - 2014-07-09)
Fastq screen is a simple application which allows you to search a large sequence dataset against a panel of differentdatabases to build up a picture of where the sequences in your data originate. It was built as a QC check forsequencing pipelines but may also have uses in metagenomicsstudies where mixed samples are expected. Although the program wasn t built with any particulartechnology in mind it is probably only really suitable forprocessing short reads due to the use of bowtie/bowtie2 as the searching application.The program generates both text and graphical output totell you what proportion of your library was able to map, either uniquely or in more than one location, against eachof the databases in your search set.
Download : http://www.bioinformatics.babraham.ac.uk/projects/fastq_screen/fastq_screen_v0.4.4.tar.gz
Usage : #fastq_screen [OPTION]... [FastQ FILE]...
FASTX-Toolkit (version 0.0.13 - 2013-04-30)
The FASTX-Toolkit is a collection of command line tools for Short-Reads FASTA/FASTQ files preprocessing.Next-Generation sequencing machines usually produce FASTA or FASTQ files, containing multiple short-reads sequences (possibly with quality information).
FigTree (version 1.4.0 - 2013-11-15)
FigTree is designed as a graphical viewer of phylogenetic trees and as a program for producing publication-ready figures. As with most of my programs, it was written for my own needs so may not be as polished and feature-complete as a commercial program. In particular it is designed to display summarized and annotated trees produced by BEAST.
Download : http://tree.bio.ed.ac.uk/software/figtree/
Usage : #figtree
FragGeneScan (version 1.30 - 2017-09-19)
FragGeneScan is an application for finding (fragmented) genes in short reads
Documentation : http://omics.informatics.indiana.edu/FragGeneScan/README
Remarque : Demande faite suite à la suite de la réunion Tiagomics du 19/09/2017
Usage : #USAGE: run_FragGeneScan.pl -genome=[seq_file_name] -out=[output_file_name] -complete=[1 or 0] -train=[train_file_name] (-thread=[number of thread; default 1])
FragGeneScanPlusPlus (version la dernière ou la suivante tant qu'à faire - 2018-09-12)
FragGeneScan en ++ rapide Attention Véro, y a un petit défi pour l'installation, sinon c'est pas drôle
Usage : # FGS++ -s [seq_file_name] -m [max_mem_use] -o [output_file_name] -w [1 or 0] -t [train_file_name] -p [thread_num] -e [1 or 0] -d [1 or 0] FGS++ -s [seq_file_name] -m [max_mem_use] -o [output_file_name] -w [1 or 0] -t [train_file_name] -p [thread_num] -e [1 or 0] -d [1 or 0]
freebayes (version v1.1.0-1-gf15e66e - 2017-02-16)
FreeBayes is a Bayesian genetic variant detector designed to find small polymorphisms, specifically SNPs (single-nucleotide polymorphisms), indels (insertions and deletions), MNPs (multi-nucleotide polymorphisms), and complex events (composite insertion and substitution events) smaller than the length of a short-read sequencing alignment.
Documentation : https://github.com/ekg/freebayes#user-manual-and-guide
Remarque : Citing freebayes:Garrison E, Marth G. Haplotype-based variant detection from short-read sequencing. arXiv preprint arXiv:1207.3907 [q-bio.GN] 2012
Usage : #freebayes -f [REFERENCE] [OPTIONS] [BAM FILES] >[OUTPUT]