Question: Should I remove duplicates?
0
gravatar for F
7 weeks ago by
F3.4k
Iran
F3.4k wrote:

Sorry,

I have a list of bam files for instance like this

HUMAN_1000Genomes_hs37d5_RNA_seq_WTSI-COLIVM_005_1pre.***dupmarked***.bam

By dupmarked likely duplicates have been marked; I want to extract raw read counts from these files by featurecounts; Do you just me to remove duplicates? How I know basically I should do that or not for extracting raw read counts?

Thank you for any help

bam next-gen duplicates • 169 views
ADD COMMENTlink modified 7 weeks ago by ATpoint15k • written 7 weeks ago by F3.4k
2

RNA-seq: Should remove duplicates in all samples of same experiment although some do not have technical duplicates? and the links there in.

ADD REPLYlink modified 7 weeks ago • written 7 weeks ago by genomax65k

Sorry, owner of data says that duplicates have not been removed rather just marked in bam files; So should I remove them now?

I should mention I also have a bam.bai for each sample like

HUMAN_1000Genomes_hs37d5_RNA_seq_WTSI-COLIVM_005_1pre.dupmarked.bam.bai
ADD REPLYlink written 7 weeks ago by F3.4k

Is this RNAseq data or something else? File name seems to indicate it is RNAseq but just to be absolutely certain.

If it is RNAseq then the post linked above has all the info you need. I will also explicitly link this: mRNA-seq quality report (fastQC): Does it mean samples have adapters and should remove duplicates?

ADD REPLYlink modified 7 weeks ago • written 7 weeks ago by genomax65k

Thank you, yes this is RNA-seq definitely

ADD REPLYlink written 7 weeks ago by F3.4k

Sorry, is it possible that these files are not normal RNA-seq files rather I should do Calling variants in RNAseq because in this paper they done that

Organoid cultures recapitulate esophageal adenocarcinoma heterogeneity providing a model for clonality studies and precision therapeutics
ADD REPLYlink modified 7 weeks ago • written 7 weeks ago by F3.4k
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