# This is an example configuration file for FastQ Screen

############################
## Bowtie, Bowtie 2 or BWA #
############################
## If the Bowtie, Bowtie 2 or BWA binary is not in your PATH, you can set 
## this value to tell the program where to find your chosen aligner.  Uncomment 
## the relevant line below and set the appropriate location.  Please note, 
## this path should INCLUDE the executable filename.

BOWTIE	/LUSTRE/apps/bioinformatica/bowtie1/bowtie
BOWTIE2 /LUSTRE/apps/bioinformatica/bowtie2/bowtie2
#BWA /usr/local/bwa/bwa



############################################
## Bismark (for bisulfite sequencing only) #
############################################
## If the Bismark binary is not in your PATH then you can set this value to 
## tell the program where to find it.  Uncomment the line below and set the 
## appropriate location. Please note, this path should INCLUDE the executable 
## filename.

#BISMARK	/usr/local/bin/bismark/bismark

############
## Threads #
############
## Genome aligners can be made to run across multiple CPU cores to speed up 
## searches.  Set this value to the number of cores you want for mapping reads.

THREADS		96

##############
## DATABASES #
##############
## This section enables you to configure multiple genomes databases (aligner index 
## files) to search against in your screen.  For each genome you need to provide a 
## database name (which can't contain spaces) and the location of the aligner index 
## files.
##
## The path to the index files SHOULD INCLUDE THE BASENAME of the index, e.g:
## /data/public/Genomes/Human_Bowtie/GRCh37/Homo_sapiens.GRCh37
## Thus, the index files (Homo_sapiens.GRCh37.1.bt2, Homo_sapiens.GRCh37.2.bt2, etc.) 
## are found in a folder named 'GRCh37'.
##
## If, for example, the Bowtie, Bowtie2 and BWA indices of a given genome reside in 
## the SAME FOLDER, a SINLGE path may be provided to ALL the of indices.  The index 
## used will be the one compatible with the chosen aligner (as specified using the 
## --aligner flag).  
##
## The entries shown below are only suggested examples, you can add as many DATABASE 
## sections as required, and you can comment out or remove as many of the existing 
## entries as desired.  We suggest including genomes and sequences that may be sources 
## of contamination either because they where run on your sequencer previously, or may 
## have contaminated your sample during the library preparation step.

## Human - sequences available from
## ftp://ftp.ensembl.org/pub/current/fasta/homo_sapiens/dna/
DATABASE	Human	/home/rgomez/bin/fastq_screen_v0.11.1/Genomes/human/hg38ome/hg38

## Ecoli- sequence available from esemble accession GCA_000967155.1
## ftp://ftp.ensemblgenomes.org/pub/bacteria/release-36/fasta/bacteria_91_collection/escherichia_coli/dna/*
DATABASE	Ecoli	/home/rgomez/bin/fastq_screen_v0.11.1/Genomes/Ecoli/Ecoli_U00096.2

## PhiX - sequence available from Refseq accession NC_001422.1
#	https://www.ncbi.nlm.nih.gov/nuccore/9626372/
DATABASE	PhiX	/home/rgomez/bin/fastq_screen_v0.11.1/Genomes/PhiX/PhiX

## Adapters - sequence derived from the FastQC contaminats file found at: www.bioinformatics.babraham.ac.uk/projects/fastqc
DATABASE	Univec	/home/rgomez/bin/fastq_screen_v0.11.1/Genomes/UniVec/UniVec

### Scerevisiae	- genome available from 
## ftp://ftp.ensembl.org/pub/release-89/fasta/saccharomyces_cerevisiae/dna
DATABASE	cerevisiae	/home/rgomez/bin/fastq_screen_v0.11.1/Genomes/s_cerevisiae/s_cerevisiae