Comments (3)
The multi-mapped reads will have mapq 0, so they will be directly filtered in Chromap's output. The default pair format does not contain MAPQ field, so it might be hard to identify multi-mapped reads based on mapq, where you can use -q 0 to include alignments with mapq 0.
from chromap.
Thank you so much for your response. Couple more question.
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Is there a way to speed up chromap? Can I run this in parallel? If yes, how much memory and nodes should I ask for?
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Is there a way to get the mapping quality for both ends for the HiC data?
from chromap.
- You can use multithreading (-t num_of_threads). It will not increase memory consumption, and the node is one.
- The mapping quality is with respect to the fragment, so you can't get the information for one read end.
from chromap.
Related Issues (20)
- "Number of mapped reads" from log file HOT 3
- [Feature Request] report number of duplicated fragments in bulk HOT 4
- Different ValidPairs rate between chromap and bowtie2 in HiC data HOT 9
- how to keep multi-mapped paires for HiC data. HOT 1
- [BUG] output to /dev/stdout HOT 6
- Understanding the multi-mapping reads and whether they are part of the bed file HOT 2
- ATAC-seq single end? HOT 3
- Coordinate system of the output fragment file? HOT 1
- [BUG] Manpage is down HOT 1
- [BUG] Support for combinatorial barcode indexing(like SHARE) not present HOT 3
- [BUG] chromap map Hi-C short reads Parameters: error threshold HOT 2
- [BUG]For HiC data, the size of SAM files outputted using Chromap is much smaller compared to those from BWA-MEM HOT 4
- Repetitive or low-quality barcode sequences in scATAC data HOT 1
- [BUG] possibly improper MD tag generation whej running atac data. HOT 3
- Mapping paired-end single-cell ATAC-Seq reads HOT 2
- why so slow? HOT 2
- Failure to load cellular barcodes containing Ns HOT 3
- Understanding the terminologies from stderr and summary HOT 11
- possible issue with /dev/stdout redirection HOT 2
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from chromap.