Hi,
We have recently received 454 targeted sequencing data, and I am having trouble finding if the data is paired-end or single-end. Where can I find this information? I am looking to detect copy number variation from the reads, and therefore need to know if I should be using the pairs or split-read info.
The original targets were enriched using one sequence capture array. The raw data reads reported fall in two regions (even though there are 4 samples, each has a separate MID tag). Do these two 'regions' correspond to different pairs?
Thank you!
We have recently received 454 targeted sequencing data, and I am having trouble finding if the data is paired-end or single-end. Where can I find this information? I am looking to detect copy number variation from the reads, and therefore need to know if I should be using the pairs or split-read info.
The original targets were enriched using one sequence capture array. The raw data reads reported fall in two regions (even though there are 4 samples, each has a separate MID tag). Do these two 'regions' correspond to different pairs?
Thank you!
Comment