Comments (15)
Hi @michieitel ,
is there a way to send us the data you used so we can try to recreate this issue on our side?
Thanks
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Hi @jmaricb -
I am currently having the same issue when trying to convert the sam output to a bam. Was there any luck in finding what the issue was?
Cheers,
Guy
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Hi @ghelman91 ,
I am currently looking into it. What dataset and reference were you using?
Thanks
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Hi @jmaricb -
I was trying to covert the sam of aligned nanopore cDNA reads mapped to the human reference genome to a bam file, similar to @michieitel above. The alignment runs fine but converting the output to a bam is the problem:
This is the command and output:
samtools view -b 191007_testNGMLR/191008_graphmap.sam > 191008_graphmap.bam
[E::sam_parse1] CIGAR and query sequence are of different length
[W::sam_read1] Parse error at line 6305
[main_samview] truncated file.
I had also used the extend cigar option just to see if I could figure out what was going on but no luck. Here is my problem line:
5f4df548-7bb6-427c-80ab-2e05238df0fc 16 chr11 6615448 0 13S9=2D14=1I3=1X21=2X1=2X10=1X15=1D24=1I9=3I442N12=1I42=1I16=586N11=1X1I68=1D60=1I55=1I3=115N1=1I1=1I19=1X1I36=6D16=1I2=1X7=1I31=1X22=1X13=2D19=147N17=1D12=1D13=8D4=1I53=1D18=197N2X5=1X55=1D28=1I4=1D6=3D10=1X1D20=1D12=999N14=1X1=2X1I23=1D1=1X11=1D18=1D5=2X1I11=2I2=1X8=1I15=1D4=1I5=1X10=2I280N1I1D5=1X15=2D1=1X12=1I9=1D17=1X2=1D3=116N36= * 0 0 GGTTACGTATTGCTGAAGGCCGGGAACACATTGCTGAAGCCACCACCACTGATATAGTCAACAATTTCATTTGTGATGAGGAAAGGTTCCTGGAAGGATGCCTCCCACTGTGGTGACATAGGGCTGAGGCAGTGTGGGAAGGTAGGGATGGAACTGGTGTCTTCCCCCAGAGACAGACCAACACCTGGCCCCAGCCTCGTCACCAGGGCTACTAGACCCAGGTGAGATGTTGGCACCAGCACTCATCAGGTACTGCACACCCAGACTGGCCTCAATCCCGGCCCGGCCCCGGCCCTGTTGTCCAACCACACGGGCTACTGATGCCCGATGTGCAAAGTTGCCACTGAAGAAAGTGCATGAACTGAGCCAGGTCTGAGTCATGGAAATACTGCTCCAGGAACTGGGCACAGGCTTGGCTGTTATTGCTGGTGCCAGAGCCCACGTCTTGTGAGGTCGTTAGCCGCTTACGGATCACAGAGGGGGCTGGCTTCCCAGATGCAGGCCTACAGTCCCTGTCACCTGCGGCTCAGACGTTGCCTCAGGGATGATGTTGGGGAAATCGGTGCAGTCCCCCCACAAAGTCCACATGGGGGCCAAGGCCTGTGGAAGCTGGTAGAGGGGGACCTTACAACATGGGTTTCCTCTGTAGGTCCTCCCACACATAGTGATGAAATCAGCCCCAGGAGCAGCAGCTCTGCTTGTCGATGCTCAGCCAGCAAGTCAGAAAGTCCTGTGTGATCACAGAACACTTCTGGGCTCCTCGGGCTGCCAAGAGCCATTTTTGCACCGTGTGGAGGGTTTGCAGGGGATGGCCTCACCAGATCAGCCACATTCTCTAGGGTCAGGTATTTCCTCCTGCATTGAAAGAGAGCTGGGATCCGACACAGCCTGCACCAGCTCCGAGAGTCTTTCCACATTCTGCTGTCCCAGGGCAAAAGGTGCAGAGACTCAGTCCTTTCTCAGGGTCCTAATGGCCCAGGGATCTGTAGCCTGGGGCAGCGTCCTCCGCTGGTCGGCTCCGGGCTGTAACTGCATTTGCCAGAGAGATGAGGGCAAAAGAGCCCCTAGGAGGCAGGCTTGGAGTCCCATTCTGCCCTTCCGCGGGATCTGTGAAGGCCGGGAACACATTGCTGGAAGTCACCACCACTGATATAGTCAAATACCTCATTTGTGACGAGGAAAGGTTCCTGAAGGATGTGCCTCCCACTGTGGTGGACATAGGGGCTGCTGGAGGCAGGGGAAGGTAGGGCGGAACTGGTGTCTTCCAGAGACAGACCAACACTCCGGCCCCACTGTCACCAGGGCTACTGAGAGACCCAGGTGGAGATGTTGGCACCAGCACTCATCAGGTACTGCACATCTAGACTGGCCTCAATCCCGCCCGGCCCCGGCCCTGTTGTCCAACCACACGGGCTACTGATGCCTGATGTGCAAAGTTGCTCACCGAAGAGGCGCATGAACTGAGCCAGGTCTGAGTCATGGAAATACTGCTCCAGTGAACTTCGGGCACAGGCTTGGCTGTTGGTTGCTGGTGCCAGAGCCCACGTCTTGTGAGGTCAAGCGCTTACGGATCACAGCAGAGGGTTACTCCCCAGATGCAGGCCTACAGTCCCTGTCACCCGCGGCTCAGGACGTTGCCTCAGTGATGATGTTGGGGAAACGGTGCAGTCCCCCCACAAAGTCCACATGGGGGCCAAGGCCTGTGAAGCTGGTAGGGACCTTTACAACATGGGTTTCCGTAGGTCCTCCCACATAGTGATGAAACTCAGCCCCAGGAGCAGCAGCTCTGCTTGTTTGATGCCCAGCCAGCAAGTCAGAAAGTCCTGTGTGATCACAGAATGGCACTTCTGGGCTCCGCTGCCAAGAGCCATTTTTGCACCGTGTGTGAGGTCAGTGATGGCCTCACTGATCAGCCACATTCTCTAGGTCAGGTATTTTCCGTATTGAGGAGAGTTTTCGATCCGACACAGCCTGCACCAGCCTGAGAGTCTTTCACATTCTGCTGTCTCAGGCAAAGCCAGAGACTCAGCTTTCTCCCTCAGGGGTCCGCACGGCCCAGGACACTCCAGCTTGGGGGCAGCGTCTCCTCTGCTGGTCGGGCTCCGCCGTAACTGCATTTTGCCAGAGAGATGAGGGCAAAGAGCCCCAGAGGCAGGCTTGGAGTCCCATTCTGCCCTTCCGCGGATCT %$(()&#((./48,:>=:899,55<C<<57767%6/-,,459000599<2@<;=A@@581.'''').:;DEED>CABC@;3IDB?>:48:8564:33=.%1E211,)((%,<+(5120,+-(2,30(,$%$&<>;>B88,-++%$$0';;603(-.8<4100/25<>@><<=;:2/;;AAB2%<<EF322)-
I might be able to directly send files if that would be helpful.
Cheers,
Guy
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The same problem here! "CIGAR and query sequence are of different length" (graphmap2 (v.0.6.01))
[bhegedus@node2 map_all_03]$ samtools view -Sb -@60 full_length_barcode01_05_scaffold_1.sam > full_length_barcode01_05_scaffold_1.bam
[E::sam_parse1] CIGAR and query sequence are of different length
[W::sam_read1] Parse error at line 13867
[main_samview] truncated file.
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@ghelman91 @michieitel @HegedusB Could you try with the newest commit? I have fixed the cigar length bug.
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dear @jmaricb , I currently encounter the same issue with ONT reads using the Graphmap2 0.6.4. release. I do not succeed in converting my .sam graphmap2 output into sorted .bam files using samtools sort nor the comments described above.
Thank you in advance.
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Can you share the dataset and the reference you are using and still getting different CIGAR and query lengths? I would like to run it and try to find the error.
Thank you.
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@menickname Well if you can, can you just send me one or several reads that have wrong CIGAR length? You don't need to send me the whole dataset. Just tell me which reference are you using then.
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DearJosip
Thank you for your quick response. Below an example of the filtered/trimmed ONT reads. The used reference genome can be found at https://www.ncbi.nlm.nih.gov/nuccore/NC_045512.2 .
@fd5bbd49-dcc4-492b-b19c-e11e853e33a5 runid=674eb540e8d54b342a1e172ff5484ba559454959 sampleid=200327_Covid-19_Artic_Protocol_restart read=1319 ch=195 start_time=2020-03-27T16:38:58Z AATTACCTGAAACTTACTTTACTCAGGTAAAAATTTACAAGAATTTCGCCCAGGAGTCAAATGGAAATTGATTTCTTAGAATTAGCTATGGATGAATTCATTGAACGGTATAGAAGGCTATGCCCAACTGAACATATCTTTATGGAGGTGCGTCATAGTCAGTTAGGTGGTTTTACATCTACTGATTGGACTAGCTAAACGTTTAAGGAATCACCTTTTGAATTAGAAGATTTTATTCCTATGGACAGTACAGTTAAAAACTATTTCATAACAGATGCACCAAACAGGTTCATCTAAGTGTGTGTTCTGTTATTGATTTATTACTTGATGATTTTGTTGTTGGAAATAATAAAATCCCAAGATTATCTGTAGTTTCTAAGGTTGAG + 4648*;;309<;8:7)@[email protected]/21@DEB;./:1334/#$.0143*-51ABCA<<1.4&&-9:9KJ>?7A000;BF?@EB?A>@)****,5=?;,,/4+01/**)5,@=?7.-)%%%%%)3(0362,+&$)38?@A;(&&&#$&4:A>@92?<;<1$1&)).37;53>C=A=;@DJDG>6A??573<>BFH:E6@F:7)FHA9?>5558?:4783;=:9766FHJFFKC>?DF@ABB43>790/5::?@<8455>?DC)>CAF>E?6.)$$')357/.0<GCD746867=?.64FHDEAC>6;335><;=6443'035;69A=>HJM4++&<<()A@C?@:979D><?DB23<0.0650<@@AGHCG>:9:@FIEA?= @2efc38c4-3d9c-491f-8772-db3fdeb8749a runid=674eb540e8d54b342a1e172ff5484ba559454959 sampleid=200327_Covid-19_Artic_Protocol_restart read=1324 ch=150 start_time=2020-03-27T16:39:01Z GGTCAATTTCTGTACAAACAACACCATCCAATTTATAGAAGTAACTGGTTTATGGTTGTTGTGTAACTGTTTTCTTTGTAGAAAACATCAATAGGACCTTTGTATTCTGAGGGACTTTGTAAGTAAAGCACCGTCTATGCAATACAAAGTTTCTTTAGAAGTTATATGTTTATAGTGACCACACTGGTAATTACCAGTGTACTCCTGCTTACAAATGTACCATGTAGAAAGTTCATACTGAGCAGGTGGTGCTGACATCATAACAAAGGTGACTCCTGTTGTACTAGATATTTTTGTAGCTTGTTTACCACACGTACAAGGTATCTGAACACCTTTCTTAAATTGTTCATAAGAGAAGTGTGCCCATGTATAACAGCAG + *(&(13.5DB@>=7:03*/224768>89?CCCG;6,9%''1:4<>@?@ID/+++.7.2<+,62))%$&%/0013;;?6444EEHD>:3?./245;?;=8>F;>BA:9?:?A<;:389?8822+:@B3:75)*)11*566@@@CA=898=>DE9A@2,+(%3)2=9997CAD?>>CEFB<>=(9559@<@C=?035:.753666&-*(%%'/3=@B@B<;45>;/)-%&&''8CE>==AH<,655=5D8966)38>==77)9;;'670746<;87-23244=><94.1710-9=A?9/5,7766680,12/.32-+,//.4,.+(3+2.3050023655/,---6:AECB?++6:*++3>?G<;;96986>>>=AFD@C@ @1d9bbe11-c3e5-4d6e-ae33-2883200d8816 runid=674eb540e8d54b342a1e172ff5484ba559454959 sampleid=200327_Covid-19_Artic_Protocol_restart read=1103 ch=454 start_time=2020-03-27T16:38:59Z TAGCGGCGTGCCTTTATGGCACGAAACACAGTGGTACGAACTTATGTACTCATTCGTTTCCGGAAAGACAGGCACGTTATTAGTTAATAGCGTACTTCTTTTTCTTGCTTTCGTGGTATTCTTGCTAGTTACACTAGCCATCCTTACTGCGCTTCGATTGTGTGCGTACTGCTGCAATATTGTTAACGTGAGTCTTGTAAAACCTTCTTTTTACGTTTACTCTCGTGTTAAAATCTAATTCTTCTAGAGTTCCTGATCTTCTGGTCTAAACGAACTAAATATTATAGTTTTCTGTTTGGAACTTTAATTTTATATATGGTTTAACAGTACTATTACCGTTGAAGAGCTAAGCTCCTTGAACAATGGAACCTAGTAG + *+*%&'&.1)/--.)%#%(%$$$$$#%%%%%42.<<=...++,?<<75/67&&?@=IED$?03/.$&*%'('%,34540'*-=8AA800G9C;<AEE@JGFGH;><,''):52''-77679>=8;=<B;.5&4589<99>22637/+1.3323832/993:57=69?<=GGFLEC;93323985@B90:19;5A@>:6;=H=162;;=>BG.+58DEGCCG.?7<;>7:>@7:58.'*')/79:<@>5HFI26C?;79?>@D<82A<ADD;''*996774439;9<:.1?@3:6264&8DAAKK9CDC>8)&#$#$%%((0%'(*+2--4(0***+,0;973)%0$#&..&976:DBCD@?EC>;;9=:;&,*080 @c46650e5-daa0-4235-8b9b-ce49c9966837 runid=674eb540e8d54b342a1e172ff5484ba559454959 sampleid=200327_Covid-19_Artic_Protocol_restart read=973 ch=467 start_time=2020-03-27T16:39:02Z AAGGTAAGAACAAGTCCTGAGTTGAATGTAAAACTGAGGATCTGAAAACTGTCAGAATTAATAAACACCACGTGTGAAAGAATTAGTGTATGCAGGGGTAATTGAGTTCTGGTTGTAAGATTAACACACTGACTAGAGACTAGTGGCAATAAAACAAGAAAAACAAACATTGTTCGTTTAGAGAACAGATCTACAAGAGATCGAAAGTTGGTTGGTA + ('33):)AABA?@@++--,.2JJCHIABB@=;<4114?;>8??))BM-(=3*.:())*-327;?;8ADAD=?B?**))'+-,-;35;<;A:978ADA;E=BCDC??G<@DCC:<>@BC=:8D@@8B/@?GID><@7DMA>;::>;:<EECFGC?<A@0LHO2+.4)&(=<GDGD>>HC-()(3=D?B;;5=5'.:;'1/.,686(((3E7:;;7=?D @e4af2786-708a-46ac-9687-b4484e6c68f7 runid=674eb540e8d54b342a1e172ff5484ba559454959 sampleid=200327_Covid-19_Artic_Protocol_restart read=1003 ch=476 start_time=2020-03-27T16:39:01Z ATGTCTTGTGCTGCCGGTACTACACACAAACTGCTTGCACTGATGACAATGCGTTAGCTTACTACAACACAACAAAGGGAGGTAGGTTTGTACTTGCACTGTTATCGATTTACAGGATTTGAAATGAAACAGATTCCCTAAGAGTGATGGAACTGGTACTATCTATGCAGAACTGGAACCACCTTGTAGGTTTGTTACGAACAATGCTTTTTCACTATGTAGAAAGTTGGATAATGATGCACTCAACAACATTATCAACAACAATGCAGAGATGGTTTATTCGCCCAGACTTTCAACCATCTCGCTGCATTATTGATAACTCATTGAGATGCATCGTGCTTCCAGCAGCATAGTGAAAAGCATTGTCTGTAACAAAAACCTACGAGGTTCCCGGTGCTGTATGGATGAGTACCATTCCATCGCTCTTGGGAATCTGGCCATTTCAAATCTGTAAATCGGATAACGTGCGTGACCTACTCCTTTTTGTTGTGTTGGCAATGGCTGGCGCATTGTCTCATCGGTACTGGCGCGATTTGTGACGCACCGGCACAGACAG + ::<??>3-80CG;@?;?>:=B<&3,.15;CFGB==<((47?;67D?>660/46<+*(*+-*,+(/77444((-::,B>>C==2>4@GD@355///%"%+,&92-)-906961008.,5?4:264+*%$#$'0''(/4$%')*$309:=<CF=8:3/))--*32/.&&5847157<?@8132558:.((:9EEB=?:..,./42300:<=;=98+)08,'$%%(((719483-)//;;>0('&27---..)()*11:()+,,*..62+++9<,%$)22*$$&,$$$$#$'$$$$)()+,*)('&$$1%&&%&$$)&%''((*(%$)3+,.%%126.%(#"#$)+%''+%&%$$33200.())())-)0-&&&&+-'%(%()$$$%#.+%0-34''($$('*,,,'*&&#**(+*))+54*+/&'+353/35=833++-+/++-23770))%%%*+)*((*&$&)/,.-(+'54//)(&+-0*0111%*+.072/*''**))'$)#%*****+&&&'*1/0$&(&$%&%##&'%'))&*$'&''--,+/..).'-$#&
I did use following command:
for READS in $(ls nanofilt*.fastq); do graphmap2 align -r ../part3_Reference_mapping/Covid-19_Ref_genome.fasta -d $READS -o ../part3_Reference_mapping/graphmap2_$READS.sam -t 36; done
The .sam file is created without any issue and seems a normal .sam file to mee. However when I want to proceed further and do further sorting and indexing, I do not get correct .bam files (only one line present in the file) and empty .bai files.
for samfiles in $(ls graphmap2_*.sam); do samtools sort $samfiles > $samfiles.bam samtools index $samfiles.bam; done
I have used the same dataset with the Graphmap pipeline and this did not give any problems in further sorting and indexing. The Graphmap2 issue appeared both on our local computer as well as our HPC infrastructure.
Thank you in advance.
Best regards,
Nick Vereecke
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Are you aligning RNA reads or DNA? If you are aligning RNA reads you should use '-x rnaseq' option. If you are aligning DNA reads then actually there is no difference between Graphmap and Graphmap2, so you could continue using Graphmap.
I will take a look anyway.
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@jmaricb we are aligning DNA sequences. We like to work with the most-up-to-date versions of the available software. Please keep me posted if the issue got solved, then I could try to run it with Graphmap2 as well.
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I will let you know. It should work with Graphmap2 too. It's just that Graphmap2 has only updates for RNA reads so it should be the same regarding DNA reads.
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Hi @jmaricb -
I was trying to covert the sam of aligned nanopore cDNA reads mapped to the human reference genome to a bam file, similar to @michieitel above. The alignment runs fine but converting the output to a bam is the problem:This is the command and output:
samtools view -b 191007_testNGMLR/191008_graphmap.sam > 191008_graphmap.bam
[E::sam_parse1] CIGAR and query sequence are of different length
[W::sam_read1] Parse error at line 6305
[main_samview] truncated file.I had also used the extend cigar option just to see if I could figure out what was going on but no luck. Here is my problem line:
5f4df548-7bb6-427c-80ab-2e05238df0fc 16 chr11 6615448 0 13S9=2D14=1I3=1X21=2X1=2X10=1X15=1D24=1I9=3I442N12=1I42=1I16=586N11=1X1I68=1D60=1I55=1I3=115N1=1I1=1I19=1X1I36=6D16=1I2=1X7=1I31=1X22=1X13=2D19=147N17=1D12=1D13=8D4=1I53=1D18=197N2X5=1X55=1D28=1I4=1D6=3D10=1X1D20=1D12=999N14=1X1=2X1I23=1D1=1X11=1D18=1D5=2X1I11=2I2=1X8=1I15=1D4=1I5=1X10=2I280N1I1D5=1X15=2D1=1X12=1I9=1D17=1X2=1D3=116N36= * 0 0 GGTTACGTATTGCTGAAGGCCGGGAACACATTGCTGAAGCCACCACCACTGATATAGTCAACAATTTCATTTGTGATGAGGAAAGGTTCCTGGAAGGATGCCTCCCACTGTGGTGACATAGGGCTGAGGCAGTGTGGGAAGGTAGGGATGGAACTGGTGTCTTCCCCCAGAGACAGACCAACACCTGGCCCCAGCCTCGTCACCAGGGCTACTAGACCCAGGTGAGATGTTGGCACCAGCACTCATCAGGTACTGCACACCCAGACTGGCCTCAATCCCGGCCCGGCCCCGGCCCTGTTGTCCAACCACACGGGCTACTGATGCCCGATGTGCAAAGTTGCCACTGAAGAAAGTGCATGAACTGAGCCAGGTCTGAGTCATGGAAATACTGCTCCAGGAACTGGGCACAGGCTTGGCTGTTATTGCTGGTGCCAGAGCCCACGTCTTGTGAGGTCGTTAGCCGCTTACGGATCACAGAGGGGGCTGGCTTCCCAGATGCAGGCCTACAGTCCCTGTCACCTGCGGCTCAGACGTTGCCTCAGGGATGATGTTGGGGAAATCGGTGCAGTCCCCCCACAAAGTCCACATGGGGGCCAAGGCCTGTGGAAGCTGGTAGAGGGGGACCTTACAACATGGGTTTCCTCTGTAGGTCCTCCCACACATAGTGATGAAATCAGCCCCAGGAGCAGCAGCTCTGCTTGTCGATGCTCAGCCAGCAAGTCAGAAAGTCCTGTGTGATCACAGAACACTTCTGGGCTCCTCGGGCTGCCAAGAGCCATTTTTGCACCGTGTGGAGGGTTTGCAGGGGATGGCCTCACCAGATCAGCCACATTCTCTAGGGTCAGGTATTTCCTCCTGCATTGAAAGAGAGCTGGGATCCGACACAGCCTGCACCAGCTCCGAGAGTCTTTCCACATTCTGCTGTCCCAGGGCAAAAGGTGCAGAGACTCAGTCCTTTCTCAGGGTCCTAATGGCCCAGGGATCTGTAGCCTGGGGCAGCGTCCTCCGCTGGTCGGCTCCGGGCTGTAACTGCATTTGCCAGAGAGATGAGGGCAAAAGAGCCCCTAGGAGGCAGGCTTGGAGTCCCATTCTGCCCTTCCGCGGGATCTGTGAAGGCCGGGAACACATTGCTGGAAGTCACCACCACTGATATAGTCAAATACCTCATTTGTGACGAGGAAAGGTTCCTGAAGGATGTGCCTCCCACTGTGGTGGACATAGGGGCTGCTGGAGGCAGGGGAAGGTAGGGCGGAACTGGTGTCTTCCAGAGACAGACCAACACTCCGGCCCCACTGTCACCAGGGCTACTGAGAGACCCAGGTGGAGATGTTGGCACCAGCACTCATCAGGTACTGCACATCTAGACTGGCCTCAATCCCGCCCGGCCCCGGCCCTGTTGTCCAACCACACGGGCTACTGATGCCTGATGTGCAAAGTTGCTCACCGAAGAGGCGCATGAACTGAGCCAGGTCTGAGTCATGGAAATACTGCTCCAGTGAACTTCGGGCACAGGCTTGGCTGTTGGTTGCTGGTGCCAGAGCCCACGTCTTGTGAGGTCAAGCGCTTACGGATCACAGCAGAGGGTTACTCCCCAGATGCAGGCCTACAGTCCCTGTCACCCGCGGCTCAGGACGTTGCCTCAGTGATGATGTTGGGGAAACGGTGCAGTCCCCCCACAAAGTCCACATGGGGGCCAAGGCCTGTGAAGCTGGTAGGGACCTTTACAACATGGGTTTCCGTAGGTCCTCCCACATAGTGATGAAACTCAGCCCCAGGAGCAGCAGCTCTGCTTGTTTGATGCCCAGCCAGCAAGTCAGAAAGTCCTGTGTGATCACAGAATGGCACTTCTGGGCTCCGCTGCCAAGAGCCATTTTTGCACCGTGTGTGAGGTCAGTGATGGCCTCACTGATCAGCCACATTCTCTAGGTCAGGTATTTTCCGTATTGAGGAGAGTTTTCGATCCGACACAGCCTGCACCAGCCTGAGAGTCTTTCACATTCTGCTGTCTCAGGCAAAGCCAGAGACTCAGCTTTCTCCCTCAGGGGTCCGCACGGCCCAGGACACTCCAGCTTGGGGGCAGCGTCTCCTCTGCTGGTCGGGCTCCGCCGTAACTGCATTTTGCCAGAGAGATGAGGGCAAAGAGCCCCAGAGGCAGGCTTGGAGTCCCATTCTGCCCTTCCGCGGATCT %$(()&#((./48,:>=:899,55<C<<57767%6/-,,459000599<2@<;=A@@581.'''').:;DEED>CABC@;3IDB?>:48:85_64:33=.%1E211,)((%,<+(5120,+-(2,30(,$%$&<>;>B88,-++%$$0';;603(-.8<4100/25<>@><<=;:2/;;AAB2%<<EF322)-$&':A:2769<AC992(,D:?/0;>,444?;>8809B00.-4>CGA>>?(C@?A1362272>7;A4-,A;:9060:<:,,.47117(94/)''$$#%%4<=<0@/9869<8;;;:=B6985=3CFF>>80=,,--7=:DECDG@A=B;514+0-530<3::6CD@5B:?BA;9,)+(-&&&33;:971//=98.-&&&%%%$$%0.-0>52795;=>88:98;%1..)(9-,,D06<.,++4:82/5,(,<217@82200500-$'2&--+-+($$$8;77?A8:6,+878576($#('%&)0++42-.*,1)=CE6;0/.**/-,55663>?>=A./.1:4>;-&7250(-(,<>>;:=.)&(++-453=A@.(#''(,08@;@;>93632/',&&&(6=C>@@BC8&7><86/-5:@4,>HF>A353@:9.@@7402%/?62;AA?<E<9622685660.-3,2_'(<))'%$&%#'/-)'&535.+#&&#'/+-.03545788-006B311+:)&'.+.;(9A@)&$',8:))0/.//$,:;>A?>>;8>1'')+&$($+,0:<6779966;-+%%+','((),,%$''94:/009&%9427%328?=>877:@667;B(:<>1=?>79/22752))66:651.,-(,6;:<=;)98754%%/%/076;:674&'76+'')41%346-+&$##,(''''%1+'%%%%)/54258782=..485?==742,-)'.2,+&//673+/.).+6&&''12/33289+('''(,0201'689:6722'&''4%589@>@?81.<$6;:E=<;<-%&%.04193217>G;::.--11%//40+AB;;42:;06%%&%$24)194@=6/21939_302,)(&&()++587))0&%,17/B)%,.-7;/.,:@<:>>$:;43=4268227896:008874(125&9$$-9$;==;8:A>;895558@@@8<8??648588>??:EC;@<<>><>;98=>;89%,-)47BDBC=;=>:.,<7892+)**)&$)0)+;=?>?:06C>???97?>9?:=A744(+./13/34&&,-.(,%&%&%'/&&#%''+(,0/.24&1-.5;<:033C@>34))&$68=@4/@=6>>@,@?6434;7>BDFC9@197'%(&%%$**1''&&5373ABB6:'035?8E:==BB3/.32$-):9A=<>B@?>=;;3852&.)+&(65:2$$$22387<A@A91/9:794,+'%$#&%&+./0//,79<=,++87<CC?9;?,-+2:332%%&-//-5++21-2-'%--,871//0&233568888846951/$$'#,249++(_,2('(+,-)%(')$$53%$%'-%%$&&;'-==00*))+,,2:;61/,,,00+6787989681/%,-.$-10420/0+589;;4001?=CBA<=9+**5)),3---'.6&&)032)'$'(&'$%&4470280-1//097==47<<;27:=388'&-6%:&+A/<>;C;<=;=07;>@:9:?9-%%6:<>6+/',-&&/>:86895865::4,',01/.0''(%9(3728))):(087;4/59.&+,68129979:@?9B99/7>16162,,6<64,''-/22>782*%($')-(.768'/19<;?=431746A?5&&834/,(((102$/054370,62>>80/-+')&$#%#$('+-+++&%%'%#.&&%32/001/2$&')'(&1--5;4443,&--31+$$%%01339(&-4'',+-((+..,37;@B/(,%*/'%)+*3))3>C>99.0/)7)8/=+2>>?>=/GBA?>@?@'%1B6AA=:;=223@0A@C@/..84:41<9=2,,++8?110/1 MD:Z:9^TT17T21T0T1T0T10T15^T33 NM:i:92 AS:i:4535 H0:i:0 ZE:f:0 ZF:f:0 ZQ:i:2188 ZR:i:135086622I might be able to directly send files if that would be helpful.
Cheers,
Guy
@HegedusB Do you solve the issue? I have the same problem:
[E::sam_parse1] CIGAR and query sequence are of different length
[W::sam_read1] Parse error at line 16323139
[main_samview] truncated file.
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Related Issues (20)
- No reads are aligned? HOT 14
- Segmentation Fault on Yeast Transcriptome HOT 9
- clang error HOT 7
- Calling help return exit-code 1
- Sam file not create it killed HOT 1
- Error building with g++ 9.3
- fail to install the graphmap2 v0.6.4 HOT 6
- Graphmap2 index in shared memory
- make installation error
- Segmentation fault
- Header not contain PG line and duplicate SQ line
- Build fails on Linux ARM64 HOT 2
- `sse` should be used only on x86_64 HOT 1
- Alignment failed
- IGV not finding sequence from bam file generated from a graphmap2 sam file
- Memory up to 140GB!!!
- Please tag a release HOT 4
- Graphmap2 can't align dRNAseq reads with U HOT 1
- Counting alignment operations error HOT 6
- Compile error? HOT 4
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from graphmap2.