Problem mapping SOLiD reads with Bowtie1
1
0
Entering edit mode
8.2 years ago
biostart ▴ 370

Hello,

Could you please have a look, what goes wrong?

I can not map old third-party SOLiD reads using Bowtie1 (it does not recognize SOLiD reads), please help! I am running Bowtie (Bowtie1) with the following command:

bowtie -t -v 2 -p 8 -m 1 -c -C hg19-Color filename.fastq filename.map

The hg19-Color is the colorspace index created using bowtie-build -C hg19.fa hg19-Color.

The .fastq file used as input was obtained by converting the corresponding .sra file downloaded from the SRA Archive using fastq-dump filename.sra.

The fastq file looks like this:

@SRR490054.1 head0094_20100208_1_EL19_K562_1pM_2_11_81_F3 length=35
T3.2230220232.1210..2201....123..222
+SRR490054.1 head0094_20100208_1_EL19_K562_1pM_2_11_81_F3 length=35
!&!%%&.65%%/;!%(1%!!)-.*!!!!*>'!!):%
@SRR490054.2 head0094_20100208_1_EL19_K562_1pM_2_11_360_F3 length=35
T0.2211222022.2321..2211....121..132
+SRR490054.2 head0094_20100208_1_EL19_K562_1pM_2_11_360_F3 length=35
!%!)(%+&(%%%&!(%&%!!&-%)!!!!&*%!!&'%
@SRR490054.3 head0094_20100208_1_EL19_K562_1pM_2_11_385_F3 length=35
T0.2233121323.2322..2011....222..223
+SRR490054.3 head0094_20100208_1_EL19_K562_1pM_2_11_385_F3 length=35
!5!%%%/=%%)'<!%.7%!!&*0)!!!!'*)!!))(

After running Bowtie, I get the following output:

Time loading forward index: 00:00:04
Time loading mirror index: 00:00:04
Time loading reference: 00:00:02
End-to-end 2/3-mismatch full-index search: 00:00:00
# reads processed: 1
# reads with at least one reported alignment: 0 (0.00%)
# reads that failed to align: 1 (100.00%)
No alignments

Do you think there is something wrong with the input fastq file, or the Bowtie parameters?

sequencing ChIP-Seq • 2.1k views
ADD COMMENT
1
Entering edit mode
8.2 years ago
jotan ★ 1.3k
bowtie -t -v 2 -p 8 -m 1 -c -C hg19-Color filename.fastq filename.map

I think it could be the smallcaps -c in the bowtie command.

According to the manual:

-c The query sequences are given on command line. i.e. <m1>, <m2> and <singles> are comma-separated lists of reads rather than lists of read files.

Bowtie would be expecting a list of reads on the command line. That's why:

# reads processed: 1
ADD COMMENT
0
Entering edit mode

Thank you, I removed the "-c", and it seems to work now.

ADD REPLY

Login before adding your answer.

Traffic: 1514 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6