How To Delete Some Rgs From One Bam File
3
0
Entering edit mode
11.2 years ago

Dear all, Before I only one sample in my analysis, but when I merge the bam file from different lane, I used the different RG. Just like the following:

@RG ID:Ptrem PL:ILLUMINA LB:Ptrem SM:Ptrem

@RG ID:PtPE14c PL:ILLUMINA LB:PtPE14c SM:PtPE14c

@RG ID:PtPE14d PL:ILLUMINA LB:PtPE14d SM:PtPE14d

@RG ID:PtPE15 PL:ILLUMINA LB:PtPE15 SM:PtPE15

@RG ID:PtPE16 PL:ILLUMINA LB:PtPE16 SM:PtPE16

@RG ID:PtPE1a PL:ILLUMINA LB:PtPE1a SM:PtPE1a

@RG ID:PtPE1a1 PL:ILLUMINA LB:PtPE1a1 SM:PtPE1a1

@RG ID:PtPE1a2 PL:ILLUMINA LB:PtPE1a2 SM:PtPE1a2

Now, I want to delete some RG from the BAM file. How could I do that? I just want to have onely one RG in the right BAM file.

• 5.6k views
ADD COMMENT
1
Entering edit mode
11.2 years ago
Irsan ★ 7.8k

picard tools addOrReplaceReadgroups

From the documentation:

Replaces all read groups in the INPUT file with a new read group and assigns all reads to this read group in the OUTPUT BAMVersion: 1.0

ADD COMMENT
0
Entering edit mode
11.2 years ago

Hi Irsan, I used the command: java -Xmx10g -jar /usr/local/bin/picard-tools-1.66/AddOrReplaceReadGroups.jar \ INPUT=new.sort.reheadered3.bam \ OUTPUT=new.sort.RG.bam \ SORT_ORDER=coordinate \ RGID=Ptrem \ RGLB=Ptrem \ RGPL=illumina \ RGPU=C063JACXX.6 RGSM=Ptrem

But I got the error: [Sun Sep 22 13:16:52 CDT 2013] net.sf.picard.sam.AddOrReplaceReadGroups done. Elapsed time: 0.02 minutes. Runtime.totalMemory()=1519058944 FAQ: http://sourceforge.net/apps/mediawiki/picard/index.php?title=Main_Page Exception in thread "main" net.sf.samtools.SAMFormatException: SAM validation error: ERROR: Record 683, Read name HWI-ST261:1:28:18847:188777#ATCACG, RG ID on SAMRecord not found in header: Ptrem1

    at net.sf.samtools.SAMUtils.processValidationErrors(SAMUtils.java:448)

    at net.sf.samtools.BAMFileReader$BAMFileIterator.advance(BAMFileReader.java:506)

    at net.sf.samtools.BAMFileReader$BAMFileIterator.next(BAMFileReader.java:487)

    at net.sf.samtools.BAMFileReader$BAMFileIterator.next(BAMFileReader.java:446)

    at net.sf.samtools.SAMFileReader$AssertableIterator.next(SAMFileReader.java:641)

    at net.sf.samtools.SAMFileReader$AssertableIterator.next(SAMFileReader.java:619)

    at net.sf.picard.sam.AddOrReplaceReadGroups.doWork(AddOrReplaceReadGroups.java:91)

    at net.sf.picard.cmdline.CommandLineProgram.instanceMain(CommandLineProgram.java:177)

    at net.sf.picard.cmdline.CommandLineProgram.instanceMainWithExit(CommandLineProgram.java:119)

    at net.sf.picard.sam.AddOrReplaceReadGroups.main(AddOrReplaceReadGroups.java:61)

What is the problem!

Thanks!

ZQ

ADD COMMENT
1
Entering edit mode

Hmm well just as the error message says, it seems there is a read with a read group ID that is not in your header. Maybe you can add VALIDATION_STRINGENCY=LENIENT (or even VALIDATION_STRINGENCY=SILENT) to your command to ignore the error and continue to replace the read group info

ADD REPLY
0
Entering edit mode
11.2 years ago

I wrote a tool name samjs: you can filter a BAM using a javascript expression: https://github.com/lindenb/jvarkit#samjs-filtering-a-sambam-file-with-javascript

$ curl -s "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/phase1/data/HG00096/exome_alignment/HG00096.mapped.illumina.mosaik.GBR.exome.20110411.bam" |\
java -jar dist/samjs.jar SE='record.readGroup.id!="SRR081241" > result.bam
ADD COMMENT

Login before adding your answer.

Traffic: 1552 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