Hi all,
I am dealing with the paired-end BAM file, and come up with many warnings like this:
WARNING: Could not find pair for HWI-ST430:177:2:1:4979:15503#0
WARNING: Could not find pair for HWI-ST430:177:2:1:5127:13427#0
WARNING: Could not find pair for HWI-ST430:177:2:1:6521:21452#0
I check the warning reads in the BAM file, and find all the warning reads have three reads with the same name. For example:
**HWI-ST430:177:2:1:4979:15503#0** 65 chr32 26100696 60 79M21S chr5 36697147 0 ACTTTGCAATTTAAGTTTTACTTACTTTTTAACTAATATACATGCCTAAAATTTACAAAAACAATAATAAAAACAACAGAACACTGGAAACATTTTTAAA >;=<>=<<=======<====;===;=======<=>>>>>><=>>==>>>>=>>>>==>?>=<<==>?>>>?>?==><=?>><=<>>>?>?=>??>?===> BD:Z:FFHFCIKKIHG@EEEHF??DGGEDGGE???DEEGGEFFFFGDHHHHGGE??FF?DGDG???EDGFGFGGF@@@FEHFEIEGFEEIJJIHBHGLJDD@EF@ MD:Z:79 PG:Z:MarkDuplicates RG:Z:Basenji BI:Z:FFIECHGIHFEAFEEHEAAFFHDFFHDAAAFEEIHFGGHGGGHHGHHHFBBGFBGGGHBBBFGHGGFGGFBBBGHIGHJGHGHFKJJJJEIKLJGHBGFB NM:i:0 AS:i:79 XS:i:19
**HWI-ST430:177:2:1:4979:15503#0** 129 chr5 36697147 60 72M28S chr32 26100696 0 ATTTGCCCCTGGGCTATTTTTTTCCTNCCATGTAAGATTCCGTTTTAAAAATGTTTCCAGTGTTCTGTTGTTTTTATTATTGTTTTTGTAAATTTTAGGC ===<=<<<<====<=>========<<!<<<=><<=>>>>>=5=>>>>>>>>>>=>>>==>=>=>>>>=?>=>>>>>>>>=?>=>>>?>>>??>??>;<=> SA:Z:chr32,26100739,-,36M64S,60,0; BD:Z:FFG@JKKFFHIIEHIGFF?????EGGEEEGHHEGEEDGFEGEGF??DE???FHEF?EGGHIFFGFEIFGGFG@@@EGGEGGGFHAAAHGJHBJJDDEHHI MD:Z:26T37T7 PG:Z:MarkDuplicates RG:Z:Basenji BI:Z:FFFBHHHFFHGGDGHGGEAAAAADFGEEEIHHGHFFFGFEGHHFBBGFBBBGHGFBEGIIIFGFEFHGFHHGCCCHIGHIGHHGDDDIIKIFKJGHGHGH NM:i:2 AS:i:65 XS:i:21
**HWI-ST430:177:2:1:4979:15503#0** 401 chr32 26100739 60 36M64H = 26100696 -79 GCCTAAAATTTACAAAAACAATAATAAAAACAACAG ===<=>>=>>===>===<=>===========>;=== SA:Z:chr5,36697147,+,72M28S,60,2; BD:Z:IHHE??FF?EGEF???FEFFFDFGE@@AHHIJFIFF MD:Z:36 PG:Z:MarkDuplicates RG:Z:Basenji BI:Z:HGHGBBFFAEGFFAAAEFFEGFEGFABBFGHGGHFF NM:i:0 AS:i:36 XS:i:22
The BAM file is alignment of HiSeq reads aligned to the reference genome using bwa, and use picard to remove redundancy. Base realignments were done using gatk.
My confusion is: 1、Why there are three reads with the same name, but have no relation? 2、Maybe the first two are treated as mate pairs and the third as a single read. So could I just ignore it?
Could eveyone help me? Many thanks for your help!
1 answer
The warnings can mean that your paired fastq files are not synchronized..
This means that you have paired reads and that one of the reads cannot find its mate in the same file (if you have only one combined file with both reads) or in the corresponding mate file.
This can occur after a stringent trimming of the sequences if you used certain trimmer programs. If you use cutadapt, trimmomatic or BBDuk, they manage the trimming process to avoid this
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your 3 reads reads have flag 65, 129 and 401. First and second are "Paired and first/Second in pair", the third is a "supplementary alignment". So this is not an error.
Hello Alphabet!
It appears that your post has been cross-posted to another site: http://stackoverflow.com/questions/36274708
This is typically not recommended as it runs the risk of annoying people in both communities.