I have a problem with counting sequences in reference to the Pindel software.
I am analyzing exome data (tumor vs. normal) and found a Short Insertion (SI) using Pindel.
One inclusion of a base (A) CTC[A]ATCA.
Total reads: 81 reads (Ref) and 83 reads (Alt) = 164 (DP), counting in tumor samples. No variant in the normal sample.
So, I used the IGV to visualize the integration (knowing that the counting of IGV can be different).
The IGV does not show sequences with insertion.
After that, I used some softwares to count/extract sequences in the insert region (counting down).
My question is: How can I confirm that the sequences are equal to Ref only the Pindel and bam-ReadCount listed?
I know Pindel realigns the sequences, but the VAF in Pindel is 50% and the other ~ 95%
- illumina HiSeq 2000
- Exome - Pairend - 150x
- Bwa Version: 0.7.5a-R405
- Human_g1k_v37.fasta reference
- Pindel version 0.2.5a1, July 23 2013.
- Atlas Indel2 v1.4.3-R158
- IndelGenotyper.36.3336
- Bam-0.4.6-ReadCount
- Samtools-0.1.19 44428cd
My Best.
I am analyzing exome data (tumor vs. normal) and found a Short Insertion (SI) using Pindel.
One inclusion of a base (A) CTC[A]ATCA.
Total reads: 81 reads (Ref) and 83 reads (Alt) = 164 (DP), counting in tumor samples. No variant in the normal sample.
So, I used the IGV to visualize the integration (knowing that the counting of IGV can be different).
The IGV does not show sequences with insertion.
After that, I used some softwares to count/extract sequences in the insert region (counting down).
HTML Code:
softwares Ref Alt DP -------------------------------------- pindel 81 83 164 atlas indel2 6 92 98 indelocator 6 92 98 bam-readcount 95 91 186 samtools view 8 92 100
I know Pindel realigns the sequences, but the VAF in Pindel is 50% and the other ~ 95%
- illumina HiSeq 2000
- Exome - Pairend - 150x
- Bwa Version: 0.7.5a-R405
- Human_g1k_v37.fasta reference
- Pindel version 0.2.5a1, July 23 2013.
- Atlas Indel2 v1.4.3-R158
- IndelGenotyper.36.3336
- Bam-0.4.6-ReadCount
- Samtools-0.1.19 44428cd
My Best.
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