Hi all from Naples,
I'm a newbie here and I hope I'm posting right.
I'm starting to work with NGS data (illumina p.e. targeted exome seq) from clinical samples;
in particular I have several datasets consisting of Tumoral and Control sequencies.
Before starting the BWA-GATK variant calling pipeline I need to verify that the samples (tumoral and control) belong to the same patient.
Is there a way to do that?
Thanks in advance.
I'm a newbie here and I hope I'm posting right.
I'm starting to work with NGS data (illumina p.e. targeted exome seq) from clinical samples;
in particular I have several datasets consisting of Tumoral and Control sequencies.
Before starting the BWA-GATK variant calling pipeline I need to verify that the samples (tumoral and control) belong to the same patient.
Is there a way to do that?
Thanks in advance.
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