miga-base 1.2.15.1 → 1.2.15.3

data/utils/FastAAI/README.md

@@ -1,84 +0,0 @@
-# FastAAI
-Fast estimation of Average Amino Acid Identities (AAI) for bacterial and viral genomes.
-Includes a module for the classification of viral genomes.
-
-## Content Table
-  * [Features](#features)
-  * [Citation](#citation)
-  * [Requirements](#requirements)
-  * [Installation](#installation)
-  * [Usage](#usage)
-  * [FAQs](#faqs)
-  * [License](#license)
-
-## Features
-Coming soon
-
-## Citation
-Coming soon
-
-## Requirements:
-- Programs:
-   - [HMMER](http://hmmer.org/) >= 3.1
-- Python >=3.6,<3.9
-- Base Python Modules:
-   - argparse
-   - datetime
-   - pathlib
-   - shutil
-   - subprocess
-   - gzip
-   - multiprocessing
-   - textwrap
-   - pickle
-   - tempfile
-   - sys
-   - functools
-- Additional Python Modules:
-   - numpy
-
-## Installation
-### Conda Installation
-FastAAIIt appears we need a bunch of pre-requisites to run FastAAI No worries, their installation using Conda is quite easy. If you don't have Conda, you can install it as follows:
-1. Download Anaconda from https://www.anaconda.com/products/individual.
-2. Run `bash Anaconda-latest-Linux-x86_64.sh` and follow the installation instructions.
-3. Once installed you can run `conda -V`. You should get the version of conda that you installed.
-
-Now, let's add the conda channels required to install the pre-requisites:
-
-```bash
-conda config --add channels conda-forge
-conda config --add channels bioconda
-conda config --add channels cruizperez
-```
-
-Then, create an environment for MicrobeAnnotator:
-
-```bash
-conda create -n fastaai hmmer prodigal numpy python=3.7 fastaai
-```
-
-And activate it:
-
-```bash
-conda activate microbeannotator
-```
-
-Both main scripts (microbeannotator and microbeannotator_db_builder) should be in your path ready for use!
-This should take care of most of the requirements except for Aspera Connect and KofamScan, which are a little more involved. Let's install those.
-
-### Pip Installation
-#Once you have installed the pre-requisites to run MicrobeAnnotator, or if you already had them and you are not using Conda, you can install MicrobeAnnotator using pip:
-
-
-## Usage
-### Database creation
-
-
-## FAQs
-
-
-
-## License
-
-See LICENSE

data/utils/enveomics/Docs/recplot2.md

@@ -1,244 +0,0 @@
-# Recruitment plots
-
-## Aims
-
-This document aims to cover the technical aspects of the recruitment plot functions in the
-`enveomics.R` package, focusing on the peak finder and gene-content diversity analyses.
-
-## Caveats
-
-This is a __*working document*__, describing  unstable and/or experimental code. The material
-here is susceptible of changes without warning, pay attention to the modification date and (if
-in doubt) the commit history. The definitions and default parameters of the functions described
-here may change in the near future as result of further experimentation or more stable
-implementations.
-
-The current document was generated and tested with the `enveomics.R` package version 1.3. To
-check your current version in R, use `packageVersion('enveomics.R')`.
-
-> **IMPORTANT**: Some of the functions described here may return unexpected results with your data.
-> Carefully evaluate all your results.
-
----
-
-## Package: `enveomics.R`
-
-The functionalities described here are provided by the `enveomics.R` package. Some features
-described here are updated more frequently than the official
-[CRAN releases](https://CRAN.R-project.org/package=enveomics.R). In order to have the latest
-updates (package HEAD), download (or update), and install this git repository.
-
-### Quick installation guide
-
-:globe_with_meridians: To install the latest stable version available in CRAN, use in R:
-
-```R
-install.packages(c('enveomics.R','optparse'))
-```
-
-:octocat: To install the latest HEAD version (potentially unstable) available in GitHub, use in R:
-
-```R
-install.packages('devtools')
-library('devtools')
-install_github('lmrodriguezr/enveomics', subdir='enveomics.R')
-```
-
----
-
-## Recruitment plots: `enve.recplot2`
-
-The first step in this analysis is the mapping of reads to the genome, processed with
-[BlastTab.catsbj.pl](http://enve-omics.ce.gatech.edu/enveomics/docs?t=BlastTab.catsbj.pl).
-We'll assume the mapping is saved in the file `my-mapping.tab` and this is also the
-prefix of the processed files.
-
-Once you have these input files (`.rec` and `.lim`), you can build the recruitment plot.
-For this, you'll have two options.
-
-### Option 1: Using the `BlastTab.recplot2.R` stand-alone script
-
-The stand-alone script
-[BlastTab.recplot2.R](http://enve-omics.ce.gatech.edu/enveomics/docs?t=BlastTab.recplot2.R)
-is the easiest option to run, and should be the preferred method if you're automating
-this analysis to process several mappings, but it doesn't offer access to advanced options.
-
-You can run it like this using two CPUs:
-
-```bash
-BlastTab.recplot2.R --prefix my-mapping.tab --threads 2 my-recplot.rdata my-recplot.pdf
-```
-
-> **NOTE 1**: It's NOT recommended to map reads against genes, the recommended strategy is to
-> map against contigs. However, if you did map reads against genes, you may want to use the
-> `--pos-breaks 0` option to use each gene as a recruitment window.
-> 
-> **NOTE 2**: If you want to plot the population peaks at this step, simply pass the
-> `--peaks-col darkred` option.
-
-Now you should have two output files: `my-recplot.rdata`, containing your `enve.RecPlot2` R
-object, and `my-recplot.pdf` with the graphical output of the recruitment plot.
-
-### Option 2: Using the `enve.recplot2` R function
-
-If you require access to advanced options, or for some other reason prefer to calculate the
-recruitment plot interactively, you can directly use the `enve.recplot2` R function. This is
-and example session in R:
-
-```R
-# Load the package
-library(enveomics.R)
-# Open the PDF
-pdf('my-recplot.pdf')
-# Build and plot the object using two threads and no peak detection
-# (to turn on peak detection, simply remove `peaks.col=NA`)
-rp <- enve.recplot2('my-mapping.tab', threads=2, peaks.col=NA)
-# Close the PDF
-dev.off()
-# Save the object
-save(rp, file='my-recplot.rdata')
-```
-
-> **IMPORTANT**: Remember to save the `enve.RecPlot2` R object (that's the last line above)
-> before closing the R session.
-
-Naturally, you may want to see what other (advanced) options you have. You can access the
-documentation of the function in R using `?enve.recplot2`.
-
----
-
-## Summary statistics
-
-Here we explore some frequently used summary statistics from recruitment plots. First, load the
-package and the `enve.RecPlot2` object you saved previously, in R:
-
-```R
-library(enveomics.R)
-load('my-recplot.rdata')
-```
-
-### Centrality measures of sequencing depth
-
-```R
-mean(enve.recplot2.seqdepth(rp)) # <- Average
-median(enve.recplot2.seqdepth(rp)) # <- Median
-enve.truncate(enve.recplot2.seqdepth(rp)) # <- 95% Central Truncated Mean
-enve.truncate(enve.recplot2.seqdepth(rp), 0.9) # <- 90% Central Truncated Mean
-```
-
-The functions above only use hits with identity above the cutoff for "in-group" (by default: 95%).
-In order to estimate the sequencing depth with a different identity cutoff, modify the cutoff first:
-
-```R
-rp98 <- enve.recplot2.changeCutoff(rp, 98) # <- Change to ≥98%
-mean(enve.recplot2.seqdepth(rp98)) # <- Average (for the new object)
-median(enve.recplot2.seqdepth(rp98)) # <- Median (for the new object)
-```
-
-### Average and median sequencing depth excluding zero-coverage windows
-
-```R
-seqdepth <- enve.recplot2.seqdepth(rp)
-mean(seqdepth[seqdepth>0]) # <- Average
-median(seqdepth[seqdepth>0]) # <- Median
-```
-
-### Average Nucleotide Identity from reads (ANIr)
-
-```R
-enve.recplot2.ANIr(rp) # <- Complete recruitment plot
-enve.recplot2.ANIr(rp, c(90,100)) # <- All reads above 90% (recommended for intra-population)
-enve.recplot2.ANIr(rp, c(95,100)) # <- Reads above 95%
-enve.recplot2.ANIr(rp, c( 0, 90)) # <- Between populations (other species)
-```
-
-### Coordinates of each sequence window with their respective sequencing depth
-
-```R
-d <- enve.recplot2.coordinates(rp)
-d$seqdepth <- enve.recplot2.seqdepth(rp)
-d
-```
-
-### Sequencing breadth (upper boundary)
-
-This estimate depends on the window size. The smaller the window size, the better the
-estimate. When the window size is 1bp, the estimate is exact, otherwise it's consistently
-biased (overestimate).
-
-```R
-mean(enve.recplot2.seqdepth(rp) > 0)
-```
-
----
-
-## Peak-finder: `enve.recplot2.findPeaks`
-
-In this step we will try to identify one or multiple population peaks corresponding to different
-sub-populations and/or composites of sub-populations.
-
-> **NOTE** This step can be performed together with the step above, but we separate it here for
-> two reasons: **(1)** This step is much more unstable but less computationally demanding than the
-> step before, so it makes sense to re-run only this part with different parameters and/or
-> package updates; and **(2)** We want to save the R objects independently, so the following steps
-> are more clear.
-
-In R:
-
-```R
-# Load the package
-library(enveomics.R)
-# Load the `enve.RecPlot2` object you saved previously
-load('my-recplot.rdata')
-# Find the peaks
-peaks <- enve.recplot2.findPeaks(rp)
-# Save the peaks R object (optional)
-save(peaks, file='my-recplot-peaks.rdata')
-# Plot the peaks in a PDF (optional)
-pdf('my-recplot-peaks.pdf')
-p <- plot(rp, use.peaks=peaks, layout=4) # <- Remove `layout=4` for the full plot
-dev.off()
-```
-
-The key function here is `enve.recplot2.findPeaks`. This function has several parameters, depending on
-the method used. To see all supported methods, use `?enve.recplot2.findPeaks`. To see all the options
-of the default method (`'emauto'`) use `?enve.recplot2.findPeaks.emauto`.
-
----
-
-## Gene-content diversity: `enve.recplot2.extractWindows`
-
-In R:
-
-```R
-# Load the package and the objects (unless you're still in the same session from the last step)
-library(enveomics.R)
-load('my-recplot.rdata')
-load('my-recplot-peaks.rdata')
-# Find the peak representing the core genome
-cp <- enve.recplot2.corePeak(peaks)
-#-----
-# The following functions illustrate how to obtain different results. Please explore the resulting
-# objects and the associated documentation
-#-----
-# Find the coordinates of windows significantly below the average sequencing depth
-div <- enve.recplot2.extractWindows(rp, cp, seq.names=TRUE)
-# Add sequencing depth
-div$seqdepth <- enve.recplot2.seqdepth(rp, as.numeric(rownames(div)))
-# Save the coordinates as a tab-delimited table
-write.table(div, 'my-low-seqdepth.tsv', quote=FALSE, sep='\t', row.names=FALSE)
-# Find all the windows with sequencing depth zero
-zero <- enve.recplot2.coordinates(rp, enve.recplot2.seqdepth(rp)==0)
-```
-
----
-
-## To do
-
-- [x] Document structure
-- [x] Package: `enveomics.R`
-- [x] Recruitment plots: `enve.recplot2`
-- [x] Summary statistics
-- [x] Peak-finder: `enve.recplot2.findPeaks`
-- [x] Gene-content diversity: `enve.recplot2.extractWindows`
-- [ ] Compare identity profiles: `enve.recplot2.compareIdentities`

data/utils/enveomics/Examples/aai-matrix.bash

@@ -1,66 +0,0 @@
-#!/bin/bash
-
-# @author  Luis M. Rodriguez-R
-# @license Artistic-2.0
-
-set -e # <- So it stops if there is an error
-function exists { [[ -e "$1" ]] ; } # <- To test *any* of many files
-
-OUT=$1		# <- Output file
-[[ -n "$1" ]] && shift
-SEQS=("$@")	# <- list of all genomes
-THR=2		# <- Number or threads
-DEF_DIST=0.9	# <- Default distance when AAI cannot be reliably estimated
-
-# This is just the help message
-if [[ $# -lt 2 ]] ; then
-echo "
-Use case: Building AAI matrices from a collection of genomes.
-
-IMPORTANT
-This script is functional, but it's mainly intended for illustrative purposes.
-Please take a look at the code first.
-
-Usage:
-$0 <output.txt> <genomes...>
-
-<output.txt>	The output AAI list, in tab-delimited form containing the
-		following columns: (1) Sequence A, (2) Sequence B, (3)
-		AAI, (4) AAI-SD, (5) Proteins used, (6) Number of proteins in
-		the smallest genome, (7) Percentage of the genome shared.
-<genomes...>	The list of files containing the genomes (at least 2).
-
-" >&2
-exit
-fi
-
-# 00. Create environment
-export PATH=$(dirname "$0")/../Scripts:$PATH
-
-# 01. Calculate AAI
-echo "[01/03] Calculating AAI"
-for i in "${SEQS[@]}" ; do
-  for j in "${SEQS[@]}" ; do
-    echo -n " o $i vs $j: "
-    AAI=$(aai.rb -1 "$i" -2 "$j" -S "$OUT.db" -t "$THR" \
-      --no-save-rbm --auto --quiet)
-    echo ${AAI:-Below detection}
-    [[ "$i" == "$j" ]] && break
-  done
-done
-
-# 02. Extract matrix
-echo "[02/03] Extracting list"
-echo -e "SeqA\tSeqB\tAAI\tSD\tN\tOmega\tFrx" > "$OUT"
-echo "select seq1, seq2, aai, sd, n, omega, (100.0*n/omega) from aai;" \
-  | sqlite3 "$OUT.db" | tr '|' '\t' >> "$OUT"
-
-# 03. Make it a distance matrix.
-echo "[03/03] Generating distance matrix"
-echo "
-source('$(dirname $0)/../enveomics.R/R/df2dist.R');
-a <- read.table('$OUT', sep = '\\t', header = TRUE, as.is = TRUE, quote = '');
-aai.d <- enve.df2dist(a, default.d = $DEF_DIST, max.sim = 100);
-write.table(as.matrix(aai.d), '$OUT.dist',
-  quote = FALSE, col.names = NA, row.names = TRUE, sep = '\\t')
-" | R --vanilla >/dev/null

data/utils/enveomics/Examples/ani-matrix.bash

@@ -1,66 +0,0 @@
-#!/bin/bash
-
-# @author  Luis M. Rodriguez-R
-# @license Artistic-2.0
-
-set -e # <- So it stops if there is an error
-function exists { [[ -e "$1" ]] ; } # <- To test *any* of many files
-
-OUT=$1		# <- Output file
-[[ -n "$1" ]] && shift
-SEQS=("$@")	# <- list of all genomes
-THR=2		# <- Number or threads
-DEF_DIST=0.9	# <- Default distance when ANI cannot be reliably estimated
-
-# This is just the help message
-if [[ $# -lt 2 ]] ; then
-echo "
-Use case: Building ANI matrices from a collection of genomes.
-
-IMPORTANT
-This script is functional, but it's mainly intended for illustrative purposes.
-Please take a look at the code first.
-
-Usage:
-$0 <output.txt> <genomes...>
-
-<output.txt>	The output ANI list, in tab-delimited form containing the
-		following columns: (1) Sequence A, (2) Sequence B, (3)
-		ANI, (4) ANI-SD, (5) Fragments used, (6) Maximum number
-		of fragments, (7) Percentage of the genome shared.
-<genomes...>	The list of files containing the genomes (at least 2).
-
-" >&2
-exit
-fi
-
-# 00. Create environment
-export PATH=$(dirname "$0")/../Scripts:$PATH
-
-# 01. Calculate ANI
-echo "[01/03] Calculating ANI"
-for i in "${SEQS[@]}" ; do
-  for j in "${SEQS[@]}" ; do
-    echo -n " o $i vs $j: "
-    ANI=$(ani.rb -1 "$i" -2 "$j" -S "$OUT.db" -t "$THR" \
-      --no-save-rbm --no-save-regions --auto --quiet)
-    echo ${ANI:-Below detection}
-    [[ "$i" == "$j" ]] && break
-  done
-done
-
-# 02. Extract matrix
-echo "[02/03] Extracting list"
-echo -e "SeqA\tSeqB\tANI\tSD\tN\tOmega\tFrx" > "$OUT"
-echo "select seq1, seq2, ani, sd, n, omega, (100.0*n/omega) from ani;" \
-  | sqlite3 "$OUT.db" | tr '|' '\t' >> "$OUT"
-
-# 03. Make it a distance matrix.
-echo "[03/03] Generating distance matrix"
-echo "
-source('$(dirname $0)/../enveomics.R/R/df2dist.R');
-a <- read.table('$OUT', sep = '\\t', header = TRUE, as.is = TRUE, quote = '');
-ani.d <- enve.df2dist(a, default.d = $DEF_DIST, max.sim = 100);
-write.table(as.matrix(ani.d), '$OUT.dist',
-  quote = FALSE, col.names = NA, row.names = TRUE, sep = '\\t')
-" | R --vanilla >/dev/null

data/utils/enveomics/Examples/essential-phylogeny.bash

@@ -1,105 +0,0 @@
-#!/bin/bash
-
-#
-# @author  Luis M. Rodriguez-R
-# @update  Mar-23-2016
-# @license artistic license 2.0
-#
-
-set -e # <- So it stops if there is an error
-function exists { [[ -e "$1" ]] ; } # <- To test *any* of many files
-
-ORG=$1 # <- Organism (see help)
-THR=2 # <- Number or threads
-
-# This is just the help message
-if [[ "$ORG" == "" ]] ; then
-echo "
-Use case: Essential genes phylogeny of a species. The essential genes are a
-collection of genes typically found in single copy in archaeal and bacterial
-genomes
-
-IMPORTANT
-This script is functional, but it's mainly intended for illustrative purposes.
-Please take a look at the code first.
-
-Usage:
-$0 <organism>
-
-<organism>	The organism to use (e.g., Streptococcus_pneumoniae).
-
-" >&2
-exit
-fi
-
-# 00. Create environment
-export PATH=$(dirname $0)/../Scripts:$PATH
-if [[ -e $ORG ]] ; then
-   echo "Cowardly refusing to overwrite $ORG, please remove archive first." >&2
-   exit 1
-fi
-mkdir $ORG
-for i in 01.proteome 02.essential 03.aln 04.cat 05.raxml 06.autoprune ; do
-   mkdir $ORG/$i
-done
-
-# 01. Download proteomes
-echo "[01/06] Downloading and guzipping data"
-RefSeq.download.bash $ORG .faa.gz "Complete Genome" $ORG/01.proteome
-rm $ORG/01.proteome/assembly_summary.txt
-for i in $ORG/01.proteome/* ; do
-   b=$(basename $i | perl -pe 's/[^A-Za-z0-9]/_/g' | perl -pe 's/_+$//')
-   if exists $i/*.faa.gz ; then
-      for j in $i/*.faa.gz ; do gunzip $j ; done
-      cat $i/*.faa > $ORG/01.proteome/$b.faa
-   fi
-   rm -R $i
-done
-
-# 02. Essential genes
-echo "[02/06] Idenfifying essential genes"
-N=0
-for i in $ORG/01.proteome/*.faa ; do # <- This loop could be parallelized
-   genomeA=$(basename $i .faa)
-   dir=$ORG/02.essential/$genomeA
-   mkdir $dir
-   HMM.essential.rb -i $i -m $dir/ -R $dir/log.txt -r $genomeA -t $THR
-   let N=$N+1
-done
-
-# 03. Find core and align groups
-echo "[03/06] Identifying core essentials and aligning groups"
-CORE_ESS=$(basename -s .faa $ORG/02.essential/*/*.faa | sort | uniq -c \
-   | awk '$1=='$N'{print $2}') 
-for b in $CORE_ESS ; do # <- This loop could be parallelized
-   cat $ORG/02.essential/*/$b.faa > $ORG/03.aln/$b.faa
-   clustalo -i $ORG/03.aln/$b.faa -o $ORG/03.aln/$b.aln #--threads=$THR
-done
-
-# 04. Concatenate alignment
-echo "[04/06] Concatenating alignments and removing invariable sites"
-Aln.cat.rb -I -c $ORG/04.cat/essential.raxcoords -i '|' $ORG/03.aln/*.aln \
-   > $ORG/04.cat/essential.aln 2> $ORG/04.cat/essential.log
-
-# 05. Run RAxML
-echo "[05/06] Inferring phylogeny"
-# You REALLY should consider running the following with more threads (-T) and,
-# if possible, multi-nodes using MPI
-cd $ORG/05.raxml
-raxmlHPC-PTHREADS -T $THR -p 1234 \
-   -s ../04.cat/essential.aln -q ../04.cat/essential.raxcoords \
-   -m PROTCATGTR -n UNUS #  IMPORTANT:	Please read the documentation of RAxML
-   			 # 		before running this line, so you know
-			 #  that you're running what you really want. Check
-			 #  options for bootstrapping and the different
-			 #  algorithms (-f). Note that -m is required, but the
-			 #  file unus.raxcoords specifies "AUTO", so RAxML will
-			 #  attempt to find the model resulting in the highest
-			 #  likelihood.
-cd ../..
-
-# 06. Autoprune
-echo "[06/06] Auto-pruning the tree"
-Newick.autoprune.R --t $ORG/05.raxml/RAxML_bestTree.UNUS --min_dist 0.001 \
-   $ORG/06.autoprune/essential-pruned.nwk
-

data/utils/enveomics/Examples/unus-genome-phylogeny.bash

@@ -1,100 +0,0 @@
-#!/bin/bash
-
-#
-# @author  Luis M. Rodriguez-R
-# @update  Oct-20-2015
-# @license artistic license 2.0
-#
-
-ORG=$1 # <- Organism (see help)
-THR=2 # <- Number or threads
-
-# This is just the help message
-if [[ "$ORG" == "" ]] ; then
-echo "
-Use case: Unus genome phylogeny of a species. The unus genome is the collection
-of orthologous groups in a set of genomes that has exactly one gene per genome,
-i.e., the core genome minus in-paralogs.
-
-IMPORTANT
-This script is functional, but it's mainly intended for illustrative purposes.
-Please take a look at the code first.
-
-Usage:
-$0 <organism>
-
-<organism>	The organism to use (e.g., Streptococcus_pneumoniae).
-
-" >&2
-exit
-fi
-
-# 00. Create environment
-export PATH=$(dirname $0)/../Scripts:$PATH
-if [[ -e $ORG ]] ; then
-   echo "Cowardly refusing to overwrite $ORG, please remove archive first." >&2
-   exit 1
-fi
-mkdir $ORG
-for i in 01.proteome 02.rbm 03.ogs 04.aln 05.cat 06.raxml ; do
-   mkdir $ORG/$i
-done
-
-# 01. Download proteomes
-echo "[01/06] Downloading and guzipping data"
-RefSeq.download.bash $ORG .faa.gz "Complete Genome" $ORG/01.proteome
-rm $ORG/01.proteome/assembly_summary.txt
-for i in $ORG/01.proteome/* ; do
-   b=$(basename $i | perl -pe 's/[^A-Za-z0-9]/_/g' | perl -pe 's/_+$//')
-   for j in $i/*.faa.gz ; do gunzip $j ; done
-   cat $i/*.faa > $ORG/01.proteome/$b.faa.tmp
-   FastA.tag.rb -i $ORG/01.proteome/$b.faa.tmp -o $ORG/01.proteome/$b.faa.tmp -d
-   rm -R $i $ORG/01.proteome/$b.faa.tmp
-done
-
-# 02. Reciprocal Best Matches
-echo "[02/06] Idenfifying Reciprocal Best Matches"
-for i in $ORG/01.proteome/*.faa ; do # <- This nested loop could be parallelized
-   genomeA=$(basename $i .faa)
-   for j in $ORG/01.proteome/*.faa ; do
-      genomeB=$(basename $j .faa)
-      rbm.rb -1 $i -2 $j -t $THR > $ORG/02.rbm/$genomeA-$genomeB.rbm
-      [[ "$i" == "$j" ]] && continue # <- Ignore if it simplifies distribution
-   done
-done
-
-# 03. Orthologous Groups
-echo "[03/06] Compiling Orthologous Groups"
-ogs.mcl.rb -d $ORG/02.rbm -o $ORG/03.ogs/pangenome.ogs -t $THR
-
-# 04. Extract unus genome and align groups
-echo "[04/06] Extracting unus genome and aligning OGs"
-ogs.extract.rb -i $ORG/03.ogs/pangenome.ogs -s $ORG/01.proteome/%s.faa \
-   -o $ORG/04.aln/ -c 1 -d 1 -p
-for i in $ORG/04.aln/*.fa ; do # <- This loop could be parallelized
-   b=$(basename $i .fa)
-   clustalo -i $i -o $ORG/04.aln/$b.aln --threads=$THR
-done
-
-# 05. Concatenate alignment
-echo "[05/06] Concatenating alignments and removing invariable sites"
-Aln.cat.rb -I -c $ORG/05.cat/unus.raxcoords -i - $ORG/04.aln/*.aln \
-   > $ORG/05.cat/unus.aln 2> $ORG/05.cat/unus.log
-
-# 06. Run RAxML
-echo "[06/06] Inferring phylogeny"
-# You REALLY should consider running the following with more threads (-T) and,
-# if possible, multi-nodes using MPI
-cd $ORG/06.raxml
-raxmlHPC-PTHREADS -T $THR -p 1234 \
-   -s ../05.cat/unus.aln -q ../05.cat/unus.raxcoords \
-   -m PROTCATGTR -n UNUS #  IMPORTANT:	Please read the documentation of RAxML
-   			 # 		before running this line, so you know
-			 # 		that you're running what you really
-			 #		want. Check options for bootstrapping
-			 #		and the different algorithms (-f). Note
-			 #		that -m is required, but the file
-			 #		unus.raxcoords specifies "AUTO", so
-			 #		RAxML will attempt to find the model
-			 #		resulting in the highest likelihood.
-