Open smondet opened 8 years ago
Wget, doing FTP to get Strelka:
Logging in as strelka ... Logged in!
==> SYST ... done. ==> PWD ... done.
==> TYPE I ... done. ==> CWD (1) /v1-branch/v1.0.14 ... done.
==> SIZE strelka_workflow-1.0.14.tar.gz ... 7002878
==> PASV ... done. ==> RETR strelka_workflow-1.0.14.tar.gz ... done.
Length: 7002878 (6.7M) (unauthoritative)
*** buffer overflow detected ***: wget terminated
======= Backtrace: =========
/lib64/libc.so.6(__fortify_fail+0x37)[0x7fad85a58ac7]
/lib64/libc.so.6(+0x10bc80)[0x7fad85a56c80]
/lib64/libc.so.6(+0x10da37)[0x7fad85a58a37]
wget[0x406a59]
wget[0x406c47]
wget[0x406eac]
wget[0x425edc]
...
GATK indel-realigner failed with:
##### ERROR ------------------------------------------------------------------------------------------
##### ERROR A USER ERROR has occurred (version 3.5-0-g36282e4):
##### ERROR
##### ERROR This means that one or more arguments or inputs in your command are incorrect.
##### ERROR The error message below tells you what is the problem.
##### ERROR
##### ERROR If the problem is an invalid argument, please check the online documentation guide
##### ERROR (or rerun your command with --help) to view allowable command-line arguments for this tool.
##### ERROR
##### ERROR Visit our website and forum for extensive documentation and answers to
##### ERROR commonly asked questions http://www.broadinstitute.org/gatk
##### ERROR
##### ERROR Please do NOT post this error to the GATK forum unless you have really tried to fix it yourself.
##### ERROR
##### ERROR MESSAGE: Invalid command line: Malformed walker argument: Could not find walker with name: RealignerTargetCreator
##### ERROR ------------------------------------------------------------------------------------------
Some chormosomes succeeded and others failed.
Restarting seems to work.
When Seq2HLA runs on non-human data, it looks like this:
# reads processed: 0
# reads with at least one reported alignment: 0 (0.00%)
# reads that failed to align: 0 (0.00%)
No alignments
/usr/lib/R/bin/exec/R: /tmp/_MEIZyDRNr/libtinfo.so.5: no version information available (required by /tmp/_MEIZyDRNr/libreadline.so.6)
Traceback (most recent call last):
File "<string>", line 1361, in <module>
File "<string>", line 126, in main
File "<string>", line 179, in mainClassI
File "<string>", line 1244, in expression
ValueError: could not convert string to float: /tmp/_MEIZyDRNr/libtinfo.so.5
seq2HLA returned -1
bwa mem failures:
[M::main_mem] read 1669990 sequences (120000049 bp)...
*** Error in `bwa': free(): invalid next size (fast): 0x00000000190c50a0 ***
ExecScript.sh: line 37: 31490 Broken pipe samtools bam2fq '/demeter/scratch/ahujaa01/ksinai-demeter/work/normal-75N-tumor-75T-noRNA-hg38/75T-read-name-sorted.bam'
31491 Segmentation fault | bwa mem -R '@RG\tID:75T-read-name-sorted.bam\tSM:75T-read-name-sorted\tLB:ga\tPL:Illumina' -t 12 -O 11 -E 4 '/demeter/scratch/ahujaa01/ksinai-demeter/reference-genome/hg38/hg38.fasta' -p -
31492 Done | samtools view -b
31493 Done | samtools sort -@ 12 -T /demeter/scratch/ahujaa01/ksinai-demeter/work/normal-75N-tumor-75T-noRNA-hg38/tumor-75T-75T.bam_bwamem-default-tmp -o '/demeter/scratch/ahujaa01/ksinai-demeter/work/normal-75N-tumor-75T-noRNA-hg38/tumor-75T-75T.bam_bwamem-default.bam'
Failure in samtools bam2fq | bwa mem
[M::mem_pestat] low and high boundaries for computing mean and std.dev: (1, 9259)
[M::mem_pestat] mean and std.dev: (1592.73, 1820.02)
[M::mem_pestat] low and high boundaries for proper pairs: (1, 12314)
[M::mem_pestat] skip orientation RR
paired reads have different names: "XYZ_0055:2:1101:1177:29462#07", "XYZ_0055:2:1101:1177:53090#07"
[mem_sam_pe] [mem_sam_pe]
When running samtools index
:
[W::bam_hdr_read] EOF marker is absent. The input is probably truncated.
samtools index: "/nfs-pool-2/biokepi/work/results-b37decoy-dna_processing_137/1b75bb82f758c48a9a243a123afc4b54_checkpoint-trials_lung_ipinivo_tumor_bams_AB653591-5_bamAB653591-5-sorted.bam" is corrupted or unsorted
From @armish:
definitely a truncated BAM (failed sorting causes this). I think you only need to remove the intermediate file and you should be good to go (that is what I do when I hit that issue)
Some tools can fail if weird ways and succeed when restarted. Where should the knowledge go?
Here is a
bwa-mem
: