And this is the output:
---------- Processing read 1 ----------
Max number of segments found: 0
Consensus construction failed!
---------- Processing read 2 ----------
Max number of segments found: 0
Consensus construction failed!
...etc
Any help would be greatly appreciated.
Thanks so much!
I am afraid that standard 16S full length library will not work. INC-Seq needs tandem repeats in the reads generated using Rolling Circle Amplification.
Is it possible to use INC-seq with the NanoPore 1D kits? I used the 1D 16S PCR barcoding kit to generate full length 16S reads.
I run this code (with my demultiplexed fasta file);
$ ./inc-seq.py -i ~/$.fasta -m 1000 -o consensus.fa
And this is the output: ---------- Processing read 1 ---------- Max number of segments found: 0 Consensus construction failed! ---------- Processing read 2 ---------- Max number of segments found: 0 Consensus construction failed! ...etc
Any help would be greatly appreciated. Thanks so much!