bug#22001: Is it possible to tab separate concatenated files?

[Assaf Gordon]

Hello Kim,

On 11/23/2015 06:09 PM, Bob Proulx wrote:
> Macdonald, Kim - BCCDC wrote:
> > For Example:
> > Concatenate the files like so:
> > > gi|452742846|ref|NZ_CAFD010000001.1| Salmonella enterica subsp., whole genome 
> > > shotgun sequenceTTTCAGCATATATATAGGCCATCATACATAGCCATATAT
> > > gi|452742846|ref|NZ_CAFD010000002.1| Salmonella enterica subsp., whole genome 
> > > shotgun 
> > > sequenceCATAGCCATATATACTAGCTGACTGACGTCGCAGCTGGTCAGACTGACGTACGTCGACTGACGTC
> > > gi|452742846|ref|NZ_CAFD010000003.1| Salmonella enterica subsp., whole genome 
> > > shotgun sequenceTATATAGATACATATATCGCGATATCAGACTGCATAGCGTCAG
> That example shows a completely different problem.  It shows that your
> input plain text files have no terminating newline, making them
> officially not plain text files but binary files.

Based on the content of your files, I'm guessing that you are working with 
mangled FASTA file.
In that case, it is possible that fixing the original files might be more 
efficient than trying to amend them later on.

The original FASTA files likely looked like so:

    >gi|452742846|ref|NZ_CAFD010000001.1| Salmonella enterica subsp., whole 
genome shotgun sequence
    TTTCAGCATATATATAGGCCATCATACATAGCCATATAT

And I'm also guessing that with some script you've removed the ">" prefix and 
joined the two lines into one.

First,
I suggest ensuring the original files have unix-style new-lines (LF) and not 
windows style (CR-LF) or Mac-style (CR).
The programs 'dos2unix' and 'mac2unix' would be able to fix it.
simply run the programs on each file, they will fix it inplace.
I would also recommend ensuring each file does end with a newline.


Second,
The FASTA id (the long text before your nucleotide sequence) contains spaces, 
and this will make downstream processing a bit of a pain.
I would recommend trimming the FASTA identifier and keeping only the first part 
(since it contains your IDs, you should have no problem
recovering the organism name later).

Example:

  $ cat 1.fa
  >gi|452742846|ref|NZ_CAFD010000001.1|  Salmonella enterica subsp., whole 
genome shotgun sequence
  TTTCAGCATATATATAGGCCATCATACATAGCCATATAT

  $ sed '/^>/s/ .*$//' 1.fa > 2.fa

  $ cat 2.fa
  >gi|452742846|ref|NZ_CAFD010000001.1|
  TTTCAGCATATATATAGGCCATCATACATAGCCATATAT

Or do it inplace for all your FA file (be sure to have a backup, though):

   for i in *.fa ; do sed -i '/^>/s/ .*$//' $i ; done


Third,
To combine and convert the files into a table (i.e. 1st column=ID, 2nd 
column=sequence),
then, assuming all your sequences are short and contained on one line, the 
following would work:

  $ cat 2.fa
  >gi|452742846|ref|NZ_CAFD010000001.1|
  TTTCAGCATATATATAGGCCATCATACATAGCCATATAT

  $ cat 3.fa
  >gi|452742846|ref|NZ_CAFD010000002.1|
  CATAGCCATATATACTAGCTGACTGACGTCGCAGCTGGTCAGACTGACGTACGTCGACTGACGTC

  $ cat *.fa | paste - - | sed 's/^>//' > final.txt

  $ cat final.txt
  gi|452742846|ref|NZ_CAFD010000001.1|  TTTCAGCATATATATAGGCCATCATACATAGCCATATAT
  gi|452742846|ref|NZ_CAFD010000002.1|  
CATAGCCATATATACTAGCTGACTGACGTCGCAGCTGGTCAGACTGACGTACGTCGACTGACGTC

the 'final.txt' will be an easy-to-work-with tabular file.


Fourth,
If you FASTA files contain multi-lined long sequences, like so:

   >gi|452742846|ref|NZ_CAFD010000002.1|
   CATAGCCATATATACTAGCTGACTGACGTCGCAGCTGGTCAGACTGACGTAC
   GTCGACTGACGTCTGTACACCACACGTTGTGACGAGCATCGACTAGCATCAG
   TTGAGCGACATCATCAGCGACGAGATCACGAGCACTAGCACTACGACTACGA

You might consider using a specialized tool to convert them to a table, such as:
 http://manpages.ubuntu.com/manpages/trusty/man1/fasta_formatter.1.html (*)
 or http://kirill-kryukov.com/study/tools/fasta-formatter/ .

Hope this helps,
 - assaf



(* shameless plug: I wrote fasta_formatter long ago)