I hereby claim:
- I am martijnvermaat on github.
- I am martijnvermaat (https://keybase.io/martijnvermaat) on keybase.
- I have a public key ASBU9sNz9RzOg8_nT4dssYbLszQejvkoSlY84KZDTpH_Dwo
To claim this, I am signing this object:
--- | |
- hosts: all | |
tasks: | |
- include_vars: vars_plain.yml | |
- assert: that="var == 'vars_plain_yml'" | |
- include_vars: vars_vaulted.yml | |
- assert: that="var == 'vars_vaulted_yml'" | |
- include_vars: vars_plain | |
- assert: that="var == 'vars_plain'" | |
- include_vars: vars_vaulted |
I hereby claim:
To claim this, I am signing this object:
# Auto SSH session aliases for hosts configured in ~/.ssh/config. | |
command_not_found_handle() { | |
if [[ ! "$1" ]] ; then | |
return 127 | |
fi | |
if ! grep -q "^Host $1\$" ~/.ssh/config; then | |
return 127 | |
fi | |
ssh $* | |
} |
These are my notes on instaling NixOS 16.03 on a Lenovo ThinkPad X1 Carbon (4th generation) with an encrypted root file system using UEFI.
Most of this is scrambled from the following pages:
When the program is started, the user is presented with a minimal pedigree consisting of a father, a mother and a child. On the left of the screen there is a slider for zooming in and zooming out.
In the top left corner three buttons can be seen, two of them (undo and redo) are greyed out. The third button is for downloading the pedigree.
In the top right corner two buttons can be seen, the left one (drawing view) is
<!doctype html> | |
<style> | |
#original input[type=range] { | |
-webkit-appearance: none !important; | |
} | |
#original input[type=range]::-webkit-slider-runnable-track { | |
height: 2px; | |
width: 100px; | |
background: red; |
#!/usr/bin/env python | |
""" | |
Modification of `python -m SimpleHTTPServer` with a fallback to /index.html | |
on requests for non-existing files. | |
This is useful when serving a static single page application using the HTML5 | |
history API. | |
""" | |
This formalisation is based on the idea that the meaning of a variant description is a set of fixed sequences projected on the referencesequence. (We call them replacements, but they can also be identities.) We explicitely do not mean the result (sequence) of applying these replacements. At least in my understanding, that is not how HGVS is intended to interpreted (and would also make it impossible to combine variants; how do you combine two plain sequences?).
# NCBI36 | |
wget ftp://ftp.ncbi.nlm.nih.gov/genomes/MapView/Homo_sapiens/sequence/BUILD.36.3/initial_release/seq_gene.md.gz -O - \ | |
| zcat | sort -t $'\t' -k 11,11 -k 2,2 > /tmp/hg18.seq_gene.sorted.md | |
mutalyzer-admin assemblies import-mapview -a hg18 /tmp/hg18.seq_gene.sorted.md 'reference' | |
mutalyzer-admin assemblies import-reference -a hg18 'NC_001807.4' | |
# GRCh37 | |
wget ftp://ftp.ncbi.nlm.nih.gov/genomes/MapView/Homo_sapiens/sequence/ANNOTATION_RELEASE.105/initial_release/seq_gene.md.gz -O - \ | |
| zcat | sort -t $'\t' -k 11,11 -k 2,2 > /tmp/hg19.seq_gene.sorted.md | |
mutalyzer-admin assemblies import-mapview -a hg19 /tmp/hg19.seq_gene.sorted.md 'GRCh37.p13-Primary Assembly' |