How to compare different illumina indices with each other to see how similar or different they are
Dear all,
I have around two groups of 15 indices of Illumina and I need to compare the two groups with each other and remove the indices that look very similar (differ by one nucleotide) from the two groups. I tried BLASTn and I provide two groups there in the fasta file format but I was not successful to run it. I get this error:
Warning: Warning: Could not calculate ungapped Karlin-Altschul parameters due to an invalid query sequence or its translation.
Is there another way for the thing I want to do?
Thank you in advance.
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Using bowtie v.1.3.1
$ more inde
>1
ACAGTGAT
>2
ACTGATAG
>3
ACTTGAGA
>4
AGTCAATA
>5
AGTTCCGG
>6
ATCACGCC
>7
ATGAGCAT
>8
ATGTCAAT
>9
ATTCCTGT
>10
CAAAAGGT
>test1
ATTCATGT
>test2
CAAACGGT
Created a bowtie index with this file, added two test sequences that differ in 1bp and then aligned
$ bowtie -x index -f inde
Setting the index via positional argument will be deprecated in a future release. Please use -x option instead.
1 + 1 0 ACAGTGAT IIIIIIII 0
2 + 2 0 ACTGATAG IIIIIIII 0
3 + 3 0 ACTTGAGA IIIIIIII 0
4 + 4 0 AGTCAATA IIIIIIII 0
5 + 5 0 AGTTCCGG IIIIIIII 0
6 + 6 0 ATCACGCC IIIIIIII 0
7 + 7 0 ATGAGCAT IIIIIIII 0
8 + 8 0 ATGTCAAT IIIIIIII 0
9 + 9 0 ATTCCTGT IIIIIIII 0
10 + 10 0 CAAAAGGT IIIIIIII 0
test1 + 9 0 ATTCATGT IIIIIIII 0 4:C>A
test2 + 10 0 CAAACGGT IIIIIIII 0 4:A>C
# reads processed: 12
# reads with at least one alignment: 12 (100.00%)
# reads that failed to align: 0 (0.00%)
Reported 12 alignments
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Are you trying to demultiplex a fastqc file? If so, there are tools for that. Else, what do you mean by 'indices'?