Entering edit mode
                    8.3 years ago
        verne91
        
    
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    20
    for example:
E00247:267:HMVT3CCXX:2:1208:32603:44398 161     chr1    29691910        25      23M4I37M87S     chrUn_gl000220  133398  -307    TTCTCTCTCTGTCTGTCTCTTTCTGCTTCTCTCTCTCTCTCTCTCTCTCCCTCTCTCTCTCTCTTTCTGCTCCTCTCTCTTTCTGTTTGTTTCTCTCCCTGTCGTTCTCCCCCCCCTCCTGTCCCTCTTTCTCTCTCTCTCGCTTCCTTGT AAAFFKKKKKKFFKKKKKKKFKKKFFF7FFFKKKKKKKKKKKKKKKKKK7<,F,,,A,,,,,,7,A,,,A,,,,7,,A7,F,,,,,,7,,77,,,F,,,,,,,,,,,,,,,(((((((,,,,,,,,,,,,,,,,,,,,,<A,,,,,,,7,, QT:Z:AAFFFFKK   BC:Z:AAGGGTGA   QX:Z:AAFFFKKKKKKKKKKK   AM:A:0  XM:A:0  RX:Z:CCGTATCTCTGCCAGG   AS:f:-79        RG:Z:NA12878:LibraryNotSpecified:1:HMVT3CCXX:2  XS:f:-80        BX:Z:CCGTATCTCTGCCAGG-1 XT:i:0  OM:i:10
The '@PG' tag:
@PG     PN:longranger.lariat    ID:lariat       CL:lariat -reads=/mnt/10x/analysis/NA12878/PHASER_SVCALLER_CS/PHASER_SVCALLER/_LINKED_READS_ALIGNER/_SORT_FASTQ_BY_BARCODE/SORT_FASTQ_BY_BC/fork0/chnk0/files/reads.fastq.gz -read_groups=NA12878:LibraryNotSpecified:1:HMVT3CCXX:5,NA12878:LibraryNotSpecified:1:HMVT3CCXX:4,NA12878:LibraryNotSpecified:1:HMVT3CCXX:7,NA12878:LibraryNotSpecified:1:HMVT3CCXX:6,NA12878:LibraryNotSpecified:1:HMVT3CCXX:1,NA12878:LibraryNotSpecified:1:HMVT3CCXX:3,NA12878:LibraryNotSpecified:1:HMVT3CCXX:2,NA12878:LibraryNotSpecified:1:HMVT3CCXX:8 -genome=/opt/10x/reference/refdata-hg19-2.1.0/fasta/genome.fa -sample_id=NA12878 -threads=4 -centromeres=/opt/10x/reference/refdata-hg19-2.1.0/regions/centromeres.tsv -trim_length=7 -output=/mnt/10x/analysis/NA12878/PHASER_SVCALLER_CS/PHASER_SVCALLER/_LINKED_READS_ALIGNER/BARCODE_AWARE_ALIGNER/fork0/chnk0/files      VN:0a2f9d6
@PG     PN:longranger.attach_phasing    ID:attach_phasing       VN:2.1.0        PP:lariat
@PG     PN:longranger   ID:longranger   VN:2.1.0        PP:attach_phasing
                    
                
                
One key important part is missing: how was the alignment generated (e.g. tools, parameters, etc)?
I added the '@PG' tag. So the aligner and parameters are there.
My guess would be this represent an average of the length for all paired-end reads for this particular fragment, but who knows? This is probably a question best asked of 10x Genomics support, I have found them to be very responsive.
10X staff today told me the TLEN is meaningless if the pairs aligned to different chromosomes.
...which begs the question on why they report TLEN to begin with in these cases; it seems like that will end up causing someone havoc down the road who doesn't run a sanity check like you have.