Hi,
I am trying to use bowtie2 to align paired end Illumina read files.
I am using following command:
./bowtie2 -a --threads 8 --n-ceil 42 --very-sensitive-local --quiet --no-sq --no-hd --np 0 --ma 1 --mp 0,0 --rdg 1,1 --rfg 1,1 --score-min L,0,0.95 -x rdp/bt2_index/rdp.db -q -1 sR1.fastq -2 sR2.fastq > bt2out.txt
The index is made from RDP II database and currently sR1.fastq and sR2.fastq contain only one read:
sR1.fastq:
@1_M01363:14:000000000-A5K8J:1:1101:8617:1211 1:N:0:16
TACGGAGGATCCGAGCGTTATCCGGA...
sR2.fastq:
@2_M01363:14:000000000-A5K8J:1:1101:8617:1211 2:N:0:16
TTCACCGTTGCCGGCGTACTCCCCAGGTGGA
The bt2out.txt file shows mostly results with sR1.fastq read header.
1_M01363:14:000000000-A5K8J:1:1101:8617:1211....
1_M01363:14:000000000-A5K8J:1:1101:8617:1211....
1_M01363:14:000000000-A5K8J:1:1101:8617:1211....
.
.
.
I am not sure how to read bowtie2 results. How can I obtain information how each matching read aligned as a pair?
Thanks
I am trying to use bowtie2 to align paired end Illumina read files.
I am using following command:
./bowtie2 -a --threads 8 --n-ceil 42 --very-sensitive-local --quiet --no-sq --no-hd --np 0 --ma 1 --mp 0,0 --rdg 1,1 --rfg 1,1 --score-min L,0,0.95 -x rdp/bt2_index/rdp.db -q -1 sR1.fastq -2 sR2.fastq > bt2out.txt
The index is made from RDP II database and currently sR1.fastq and sR2.fastq contain only one read:
sR1.fastq:
@1_M01363:14:000000000-A5K8J:1:1101:8617:1211 1:N:0:16
TACGGAGGATCCGAGCGTTATCCGGA...
sR2.fastq:
@2_M01363:14:000000000-A5K8J:1:1101:8617:1211 2:N:0:16
TTCACCGTTGCCGGCGTACTCCCCAGGTGGA
The bt2out.txt file shows mostly results with sR1.fastq read header.
1_M01363:14:000000000-A5K8J:1:1101:8617:1211....
1_M01363:14:000000000-A5K8J:1:1101:8617:1211....
1_M01363:14:000000000-A5K8J:1:1101:8617:1211....
.
.
.
I am not sure how to read bowtie2 results. How can I obtain information how each matching read aligned as a pair?
Thanks
Comment