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Full Discussion: Creating a shortcut
Top Forums Shell Programming and Scripting Creating a shortcut Post 302663689 by kylle345 on Thursday 28th of June 2012 11:15:32 AM
Old 06-28-2012
Hi thanks for replying. Yes that definitely works and I am slowly getting to the final stage.

Here is the new code that I have. Yet again there are still problems but I think a minor tweek from you experts can solve it.

Code:
awk 'NR==FNR{a[$1];next}($1 in a){print}' 1st.txt *filmatch.txt | awk '{ M=NF; for(N=4; N<=NF; N++) T[N]+=$N } END {printf("%f", T[4]/NR);for(N=5; N<=M; N++) printf("\t%f", T[N]/NR);printf("\n");}' > output.txt

What the above currently does is match all files based on 1st.txt and puts them into ONE output file. *filmatch.txt is made up of numerous files (2.txt, 3.txt, 4.txt etc.) and I want to include their name in the final file.

right now the current output looks like this (basically just the values that I want averaged):

Code:
0.068808	0.067252	0.068956	0.068141	0.068563	0.069272	0.070322	0.070029	0.069015	0.071708	0.071292	0.069931	0.071829	0.070628	0.069996	0.071036	0.070910	0.071590

But I want it to look like this:

Code:
1st.txt 0.068808	0.067252	0.068956	0.068141	0.068563	0.069272	0.070322	0.070029	0.069015	0.071708	0.071292	0.069931	0.071829	0.070628	0.069996	0.071036	0.070910	0.071590

2nd.txt 0.068808	0.067252	0.068956	0.068141	0.068563	0.069272	0.070322	0.070029	0.069015	0.071708	0.071292	0.069931	0.071829	0.070628	0.069996	0.071036	0.070910	0.071590

etc...

If you can get this to work then it would be great.

Thanks
 

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FASTX_QUALITY_STATS(1)						   User Commands					    FASTX_QUALITY_STATS(1)

NAME
fastx_quality_stats - FASTX Statistics DESCRIPTION
usage: fastx_quality_stats [-h] [-N] [-i INFILE] [-o OUTFILE] Part of FASTX Toolkit 0.0.13.2 by A. Gordon (gordon@cshl.edu) [-h] = This helpful help screen. [-i INFILE] = FASTQ input file. default is STDIN. [-o OUTFILE] = TEXT output file. default is STDOUT. [-N] = New output format (with more information per nucleotide/cycle). The *OLD* output TEXT file will have the following fields (one row per column): column = column number (1 to 36 for a 36-cycles read solexa file) count = number of bases found in this column. min = Lowest quality score value found in this column. max = Highest quality score value found in this column. sum = Sum of quality score values for this column. mean = Mean quality score value for this column. Q1 = 1st quartile quality score. med = Median quality score. Q3 = 3rd quartile quality score. IQR = Inter-Quartile range (Q3-Q1). lW = 'Left-Whisker' value (for boxplotting). rW = 'Right-Whisker' value (for boxplotting). A_Count = Count of 'A' nucleotides found in this column. C_Count = Count of 'C' nucleotides found in this column. G_Count = Count of 'G' nucleotides found in this column. T_Count = Count of 'T' nucleotides found in this column. N_Count = Count of 'N' nucleo- tides found in this column. max-count = max. number of bases (in all cycles) The *NEW* output format: cycle (previously called 'column') = cycle number max-count For each nucleotide in the cycle (ALL/A/C/G/T/N): count = number of bases found in this column. min = Lowest quality score value found in this column. max = Highest quality score value found in this column. sum = Sum of quality score values for this column. mean = Mean quality score value for this column. Q1 = 1st quartile quality score. med = Median quality score. Q3 = 3rd quartile quality score. IQR = Inter-Quartile range (Q3-Q1). lW = 'Left-Whisker' value (for boxplotting). rW = 'Right-Whisker' value (for boxplotting). SEE ALSO
The quality of this automatically generated manpage might be insufficient. It is suggested to visit http://hannonlab.cshl.edu/fastx_toolkit/commandline.html to get a better layout as well as an overview about connected FASTX tools. fastx_quality_stats 0.0.13.2 May 2012 FASTX_QUALITY_STATS(1)
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