# HG changeset patch # User davidvanzessen # Date 1482333799 18000 # Node ID 44ec2a1009fc7936902be591c3014450e2bf2992 # Parent cbce7f35f8b0a5557a44f7687f13a3ee9ebaa366 Uploaded diff -r cbce7f35f8b0 -r 44ec2a1009fc results_footer.html --- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/results_footer.html Wed Dec 21 10:23:19 2016 -0500 @@ -0,0 +1,75 @@ + + +
+ +

Table showing +the number of sequences identified for each samples and the number of sequences +in which no MID tag could be matched. In addition, multiple files can be +downloaded for each sample.

+ +

FASTQ: +Downloads a FASTQ file with all the sequences that are linked to the sample. +Sequences have not been trimmed.

+ +

FASTA: +Downloads a FASTA file with all the sequences that are linked to the sample. +Sequences have not been trimmed.

+ +

Trimmed FASTA: +Downloads a trimmed FASTA file with all the sequences that are linked to the +sample. Sequences are trimmed according to the settings entered at the barcodes +section of the main page of the demultiplex tool.

+ +

FASTQC: The +sequences of each individual sample automatically is analysed using FASTQC. +Clicking “Report” opens a new page containing all quality control results of +the analysis of FASTQC. (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/)

+ +

 

+ +
diff -r cbce7f35f8b0 -r 44ec2a1009fc wrapper.sh --- a/wrapper.sh Wed Dec 21 10:07:42 2016 -0500 +++ b/wrapper.sh Wed Dec 21 10:23:19 2016 -0500 @@ -64,4 +64,7 @@ python $dir/trim.py --input "$file.fasta" --output "${file}_trimmed.fasta" --start "${trim_start[$barcode]}" --end "${trim_end[$barcode]}" echo "$barcode$count$file.fastq$file.fasta${file}_trimmed.fastaReport" >> $output done < output.txt -echo "" >> $output + +echo "" >> $output +cat $dir/results_footer.html >> $output +echo "" >> $output