Cheatography
https://cheatography.com
A quick seqkit cheat sheet for the commands I use the most
grep
-f |
pattern file |
-p |
search pattern |
-v |
invert (non-matching) |
-r |
patterns use regular expression |
-n |
by name |
-s |
by seq |
-i |
ignore case |
search sequences by pattern(s) of name or sequence motifs
fx2tab
-n |
print names |
-i |
print id (instead of full header) |
-g |
print gc content |
-G |
print gc-skew |
-l |
print length |
-B |
print base content (e.g. -B AT -B N) |
sort
-l |
by length |
-n |
by full name (not id) |
-s |
by sequence |
-r |
reverse |
|
|
stats
-a |
all |
-T |
tabular (machine readable |
-j |
number of threads |
split
-i |
by id |
-p |
into # parts |
-s |
by size |
-O |
output directory (def. is $infile.split) |
use split2 for fastq/paired end (-1 + -2 for paired end)
seq
-m |
min. length of reads to output e.g. 500 for reads over 500bp |
-M |
max. length of reads to output e.g. 500 for reads under 500bp |
-n |
only print read names |
-w |
defines line width, 0 for no wrap (i.e. to turn into one-line fastx) |
-i |
print ID instead of full head (shorten ID) |
other
faidx |
Create fasta index file |
fq2a |
fastq to fasta |
rmdup |
remove duplicated sequences |
|
Created By
Metadata
Comments
No comments yet. Add yours below!
Add a Comment
Related Cheat Sheets