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ping-legacy's Issues

"Use of uninitiazed value ..." message in ping_run_all()

When I run ping_run_all() on the attached paired end files after changing the first few lines of PING_run_all.R

  sample.location = "input/",
  fastq.pattern.1 = "_R1_001.fastq.gz",
  fastq.pattern.2 = "_R2_001.fastq.gz",
  bowtie.threads = 7,
  results.directory = "output/"

I get

----- Getting PING_grabber ready -----

PING_sequences/ directory created.

Found sequences: 
test1


Running MrGrabWaller on: test1 

bowtie2 -p7 --trim5 3 --trim3 7 -L 20 -i S,1,0.5 --score-min L,0,-0.187 -I 75 -X 1000 -x Resources/grabber_resources/Filters/mrG/output -1 input/test1_R1_001.fastq.gz -2 input/test1_R2_001.fastq.gz -S test1.temp --al-conc-gz PING_sequences/test1_KIR_%.fastq.gz --un dump.meUse of uninitialized value $bt2_args[17] in join or string at /usr/local/bin/bowtie2 line 423.
Use of uninitialized value $bt2_args[18] in join or string at /usr/local/bin/bowtie2 line 423.
Use of uninitialized value in exists at /usr/local/bin/bowtie2 line 81.
Use of uninitialized value in exists at /usr/local/bin/bowtie2 line 81.
Use of uninitialized value $bt2_args[17] in join or string at /usr/local/bin/bowtie2 line 459.
Use of uninitialized value $bt2_args[18] in join or string at /usr/local/bin/bowtie2 line 459.
20000 reads; of these:
  20000 (100.00%) were paired; of these:
    1056 (5.28%) aligned concordantly 0 times
    15 (0.07%) aligned concordantly exactly 1 time
    18929 (94.64%) aligned concordantly >1 times
    ----
    1056 pairs aligned concordantly 0 times; of these:
      0 (0.00%) aligned discordantly 1 time
    ----
    1056 pairs aligned 0 times concordantly or discordantly; of these:
      2112 mates make up the pairs; of these:
        2080 (98.48%) aligned 0 times
        0 (0.00%) aligned exactly 1 time
        32 (1.52%) aligned >1 times
94.80% overall alignment rate


MrGrabwaller is complete. Extracted reads are deposited in the PING_sequences folder.
fastq.patterns have been adjusted to _KIR_1.fastq(.gz) and _KIR_2.fastq(.gz).
----- Getting PING ready -----

Results being saved to output/ 

Found sequences: 
test1_KIR

Setting results directory to output/

----- Running KFF -----

Building primer table. 

Counting primers in: 
test1_KIR_1
Taking input= as a system command ('zcat PING_sequences/test1_KIR_1.fastq.gz') and a variable has been used in the expression passed to `input=`. Please use fread(cmd=...). There is a security concern if you are creating an app, and the app could have a malicious user, and the app is not running in a secure environment; e.g. the app is running as root. Please read item 5 in the NEWS file for v1.11.6 for more information and for the option to suppress this message.
zcat: can't stat: PING_sequences/test1_KIR_1.fastq.gz (PING_sequences/test1_KIR_1.fastq.gz.Z): No such file or directory
Error: subscript out of bounds
In addition: Warning messages:
1: In dir.create(save_to) : 'output' already exists
2: In dir.create(save_to) : 'output' already exists
3: In fread(paste("zcat", inFile), sep = "\n", nrows = read.cap, header = FALSE) :
  File '/var/folders/35/dkcf9qv55hn3sfhvvstf1yy80000gn/T//RtmpDMH95n/file9bd0557acc4d' has size 0. Returning a NULL data.table.

Any suggestions? I am running the latest code on OSX 10.15.4. The file 'PING_sequences/test1_KIR_1.fastq.gz' does exist.

test1_R1_001.fastq.gz
test1_R2_001.fastq.gz

KIR_allele_info_contigstats

Hi,

In the function build_mira_counts in PING_gc_caller_v1.1.R, there is the following line:

mira_filepath <- "KIR_allele_assembly/KIR_allele_d_info/KIR_allele_info_contigstats.txt"

I haven't been able to locate this file or directory. Is it created in a previous step? Alternatively, is it available on the Github somewhere? Thanks very much for your help.

running on non-paired sequences

The documentation and script PING_run_all.R show that paired fastqs are required for input. Is there a work-around or any way to run on non-paired data?

running allele caller without 2DS1, 2DS2, and 3DP1 data output

I have run 48 cases of target enrichment sequencing of IHWG standard DNA and analyzed by PING.
All cases output their KIR allele in allele caller except 2DS1, 2DS2, 3DP1.
Although these samples have been approved of these genes existence in KFF results and MIRA results.
In the script of PING_allele_caller, there is no loci caller of 2DS1, 2DS2, and 3DP1.
But I found the reference of 2DS1, 2DS2 in resource directory of caller_resources.
Does these version of PING can't make allele calling of these three genes?

Error while running PING

Hi,

I tried running the pipeline and getting following error:

ping_run_all(sample.location="/projects/Clinomics/DATA/Sample_CL0080_T1D_E2_HW7J3BGXY/", fastq.pattern.1="_R1.fastq.gz", fastq.pattern.2="_R2.fastq.gz",bowtie.threads=10,results.directory="/projects/scratch/PING/")
----- Getting PING_grabber ready -----

PING_sequences/ directory created.

Found sequences:
Sample_CL0080_T1D_E2_HW7J3BGXY

Running MrGrabWaller on: Sample_CL0080_T1D_E2_HW7J3BGXY

bowtie2 -p10 --trim5 3 --trim3 7 -L 20 -i S,1,0.5 --score-min L,0,-0.187 -I 75 -X 1000 -x Resources/grabber_resources/Filters/mrG/output -1 /projects/Clinomics/DATA/Sample_CL0080_T1D_E2_HW7J3BGXY/Sample_CL0080_T1D_E2_HW7J3BGXY_R1.fastq.gz -2 /projects/Clinomics/DATA/Sample_CL0080_T1D_E2_HW7J3BGXY/Sample_CL0080_T1D_E2_HW7J3BGXY_R2.fastq.gz -S Sample_CL0080_T1D_E2_HW7J3BGXY.temp --al-conc-gz PING_sequences/Sample_CL0080_T1D_E2_HW7J3BGXY_KIR_%.fastq.gz --un dump.me(ERR): Could not open output file 'Sample_CL0080_T1D_E2_HW7J3BGXY.temp' for writing.
Exiting now ...

on the system I am running the pipeline I am a user and don't have write permission on the location PING is installed to.

success with exome sequencing?

I'm wondering if you or others have had success running PING from whole exome sequencing? Do the probes tend to capture enough KIR region reads or do they mostly get missed?

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