cyklee

# Quick conversion from latitude/longitude formats ("degrees decimal minutes" or "degrees minutes seconds") to decimal coordinates.
# This conversion needs to be verified since I know little of geodesy

# Load the list data
LL <- read.delim("~/Dropbox/POLAR GRADIENTS/latitude_longitude.tsv", quote="")
library(sp)

as.numeric(char2dms(as.character(LL$Latitude), chd="d", chm = "'", chs = "\""))
as.numeric(char2dms(as.character(LL$Longitude), chd="d", chm = "'", chs = "\""))

cyklee

# Run me first to count the lengths of sequences in FASTQ files in the directory.
# This script is linebreak dependent, therefore no interleaving is allowed.
# NR%4==2 means print every 4th line starting from 2nd
# NR%2==0 means print every 2nd line starting from 2st (note the 0)

for i in *.fastq; do
cat $i | awk '{if(NR%4==2) print length($1)}' >  ${i}.readslength.txt
done

for i in *.fasta; do

cyklee

# This is an exercise in 16S rRNA gene sequence processing in R

library(phyloseq)
library(dada2)
library(Biostrings)

# Load OTU table generated by USEARCH with phyloseq
# Load the "classic" OTU table converted from .uc to .txt via uc2otutab.py
otuFile <- read.delim("example_readmap.txt", header=TRUE, row.names=1)
otu <- otu_table(otuFile,taxa_are_rows = TRUE)

cyklee

mv ./*/**/*(.D) ./

cyklee

# In order to using the plotting script in `compare_alpha_diversity.py` we need to convert the output from `alpha_diversity.py`
# to resemble that coming out of `collate_alpha.py`, which involves transposing the column of sample name and ouput to rows.
# In theory, we will have only two rows, one for site names and one for the alpha diversity.

# Here's the transposition workflow for my own reproducibility purposes:

awk '
{ 
    for (i=1; i<=NF; i++)  {
            a[NR,i] = $i

cyklee

tmux cheat sheet

(C-x means ctrl+x, M-x means alt+x)

Prefix key

The default prefix is C-b. If you (or your muscle memory) prefer C-a, you need to add this to ~/.tmux.conf:

remap prefix to Control + a

cyklee

#!/bin/zsh
# Load OTU table generated by fastq2biom into phyloseq
# I'm converting from HDF5 to JSON format because otherwise phyloseq would drop low abundance OTU for me 
biom convert -i ${project}_tax.biom -o ${project}_tax.json --to-json

# I have problem where the "id" and "type" field values are malformed:
# My conversion output: "b'No Table ID'" & "b'OTU table'"
# Should be: "No Table ID" & "OTU table"
# Fixing this with sed:
sed -i "s/b'//g; s/'//g" ${project}_tax.json

cyklee

su
systemctl enable vboxservice
systemctl start vboxservice
groupadd vboxsf
gpasswd -a $USER vboxsf
exit

sudo usermod -aG vboxsf $(whoami) 
# Log off & log back in

cyklee

# https://www.biostars.org/p/49820/
# https://github.com/mdshw5/pyfaidx can be used as a drop-in replacement
xargs samtools faidx test.fa < names.txt

cyklee

# Port forwarding using miniUPNP client
# Use crontab to automate upon reboot
# https://superuser.com/questions/634628/is-there-a-script-to-add-port-forwarding-rule-in-home-router

upnpc -a `ifconfig wlan0 | grep "inet addr" | cut -d : -f 2 | cut -d " " -f 1` 22 22 TCP
upnpc -a `ifconfig wlan0 | grep "inet addr" | cut -d : -f 2 | cut -d " " -f 1` 5900 5900 TCP
upnpc -a `ifconfig wlan0 | grep "inet addr" | cut -d : -f 2 | cut -d " " -f 1` 9091 9091 TCP