Comments (2)
Hi @apcamargo ,
Thank you for your post. However, I am not sure if I understand the request clearly.
Would you mind explaining a little bit more?
from pufferfish.
Sure, @fataltes!
Here's Puffaligner's (using --bestStrata
) samtools flagstat
output:
214688504 + 0 in total (QC-passed reads + QC-failed reads)
50488220 + 0 secondary
0 + 0 supplementary
0 + 0 duplicates
125913389 + 0 mapped (58.65% : N/A)
164200284 + 0 paired in sequencing
82100142 + 0 read1
82100142 + 0 read2
83360444 + 0 properly paired (50.77% : N/A)
83360444 + 0 with itself and mate mapped
6101721 + 0 singletons (3.72% : N/A)
0 + 0 with mate mapped to a different chr
0 + 0 with mate mapped to a different chr (mapQ>=5)
Here's Bowtie2's (using -k 15
):
241492571 + 0 in total (QC-passed reads + QC-failed reads)
77292287 + 0 secondary
0 + 0 supplementary
0 + 0 duplicates
159016623 + 0 mapped (65.85% : N/A)
164200284 + 0 paired in sequencing
82100142 + 0 read1
82100142 + 0 read2
74243714 + 0 properly paired (45.22% : N/A)
77436030 + 0 with itself and mate mapped
4288306 + 0 singletons (2.61% : N/A)
2489036 + 0 with mate mapped to a different chr
2027014 + 0 with mate mapped to a different chr (mapQ>=5)
Puffaligner's with mate mapped to a different chr
is 0, meaning that there are no pairs with reads that mapped to different references.
Essentially, I'm interest in alignments where the 7th field is not =
, for example:
HISEQ13:355:CBN0FANXX:7:1101:17319:1971 97 k147_2000503 17 38 150M k147_584177 66 0 CGGCGGACTAAGGCTCTATAATTTCAATTTTTCACCAGACTAAGTAATCCATGAAGAAACTCATTGCAGCACTGGCTTCCAGTGTTCTGGTGATGTCCGCCGCCGTCGCCCAGACGCTGCCGGCGCCGACCATCGCCGCCAAATCGTGGC =ABBGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGFGGGGGGGGGGGGGGGGGGGFGG>GEGGGGGGDGFGGCGDGDGGGGG<DGGGGGGGBGGGGGGGGGGGGGGGGGGGGGGGGGG@ AS:i:0 XN:i:0 XM:i:0 XO:i:0 XG:i:0 NM:i:0 MD:Z:150 YT:Z:UP
from pufferfish.
Related Issues (20)
- installing without root HOT 13
- kquery, missing command HOT 28
- Please consider converting ExternalProject_Add to git submodules
- Puffaligner fasta file HOT 1
- [Compile error] cannot open output file cedar: Is a directory
- No executable after installing HOT 1
- Pufferfish doesn't build within a conda environment (which has all the prerequisites) due to failed build of tslib from SeqLib HOT 9
- Add description to help that pufferfish index supports gzipped FASTA reference file
- Pufferfish index `--decoys <decoy_list>` option doesn't tell you how to provide a list of FASTA files HOT 3
- Pufferfish index decoy option fixFasta doesn't recognize FASTA header(s) and fails HOT 2
- xz-5.2.2.tar.gz: FAILED HOT 2
- Parallelize fixFasta
- Output unmapped reads
- Align command fails or shows help when options aren't in a specific order HOT 1
- PuffAligner significantly slower at mapping and thread usage is much less than specified when running with `--compressedOutput` HOT 1
- Would Pufferfish index and align be more efficient if I merged each genome into a single contig and FASTA entry per genome? HOT 1
- Cedar segfaults with SAM files HOT 1
- Create and query an index of many human genomes?
- can't install pufferfish
- Fails to compile on IBM Power architecture (ppc64le)
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