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Exit: Error: Directory Hierarchy of rawdata '/home/genome/Caulobacter/HiC_data/' is not correct. No '.fastq(.gz)' files detected #168
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Hi You will also need to update the config file with And please, check to the index files are Best |
Dear nservant, |
Hi,
Which HiC-Pro version are you using ?
Could you show me the data organization, and the config file.
Thanks
N
Le 09/03/2019 à 18:59, GitHub-Lujianjun a écrit :
…
Dear Qingdong:
I also have the some quesion you had described before. I have tried
many times according to @navrant's advises, but still not work! The
only difference from you is that my HiC data are compressed in "
*fastq.gz". BTW, I'm curious about that "PAIR1_EXT = _1" and
"PAIR1_EXT = _2",why not the full name like "PAIR1_EXT = SRR824846_1"
and "PAIR1_EXT =SRR824846_2" ?
Do you have any ideas for me?
Thankyou so much!
JJLu.
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The same happens to me, but they are there.. bin/HiC-Pro -i /gpfs/project/projects/qggp/Potatodenovo/data/HiC/sample1 -o /gpfs/project/projects/qggp/Potatodenovo/results/10x/HiC-pro -c config-hicpro.txt -p ll /gpfs/project/projects/qggp/Potatodenovo/data/HiC/sample1 |
Dear Viriatoll,
I was also facing similar kind of issue recently.
When I checked the log file of HiC-Pro, I noticed that my system created a
hidden system/temp folder with the same directory name, and HiC-Pro
actually looking for those fastq files on that hidden system/temp folder.
Deleting those hidden system/temp directories solved my issue. You can also
try the same, to resolve your issue.
Have a good day.
Sourav Ghosh
…On Tue, Jul 9, 2019 at 4:59 PM ViriatoII ***@***.***> wrote:
The same happens to me, but they are there..
ll /gpfs/project/projects/qggp/Potatodenovo/data/HiC/sample1
-rwxrwx--- 1 riesd QGGP 46656175972 May 4 04:19 HiC_R1.fastq
-rwxrwx--- 1 riesd QGGP 46640555968 May 4 04:34 HiC_R2.fastq
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Please run HiC-Pro with |
I encounter the same issue, I have only one sample,and construst the reads directory like |
This is the first result when I google the issue. I think the issue for wuxiaopei0509 is that HiC Pro doesn't accept gzipped fastq files. I could be wrong, but I didn't find anything contradictory in the documentation. |
Dear,
When I use Hic-Pro (HiC-Pro_2.10.0) on (linux 3.10.0-693.21.1.el7.x86_64 #1 x86_64 GNU/Linux) with the code "HiC-Pro -i /home/genome/Caulobacter/HiC_data/ -o /home/genome/Caulobacter/HiC_data_out -c /home/genome/Caulobacter/config-hicpro.txt", there is an error "Exit: Error: Directory Hierarchy of rawdata '/home/genome/Caulobacter/HiC_data/' is not correct. No '.fastq(.gz)' files detected".
while the fastq files just in this file
"ll /home/genome/Caulobacter/HiC_data/
总用量 9965776
-rw-rw-r-- 1 zengqd zengqd 5102474162 7月 27 20:12 SRR824846_1.fastq
-rw-rw-r-- 1 zengqd zengqd 5102474162 7月 27 20:12 SRR824846_2.fastq
"
my config-hicpro.txt as:
cat config-hicpro.txt
Please change the variable settings below if necessary
#########################################################################
Paths and Settings - Do not edit !
#########################################################################
TMP_DIR = tmp
LOGS_DIR = logs
BOWTIE2_OUTPUT_DIR = bowtie_results
MAPC_OUTPUT = hic_results
RAW_DIR = rawdata
#######################################################################
SYSTEM AND SCHEDULER - Start Editing Here !!
#######################################################################
N_CPU = 40
LOGFILE = hicpro.log
JOB_NAME =
JOB_MEM =
JOB_WALLTIME =
JOB_QUEUE =
JOB_MAIL =
#########################################################################
Data
#########################################################################
PAIR1_EXT = _R1
PAIR2_EXT = _R2
#######################################################################
Alignment options
#######################################################################
FORMAT = phred33
MIN_MAPQ = 0
BOWTIE2_IDX_PATH = /home/genome/Caulobacter
BOWTIE2_GLOBAL_OPTIONS = --very-sensitive -L 30 --score-min L,-0.6,-0.2 --end-to-end --reorder
BOWTIE2_LOCAL_OPTIONS = --very-sensitive -L 20 --score-min L,-0.6,-0.2 --end-to-end --reorder
#######################################################################
Annotation files
#######################################################################
REFERENCE_GENOME = bacteria
GENOME_SIZE = bacteria.size
CAPTURE_TARGET =
#######################################################################
Allele specific analysis
#######################################################################
ALLELE_SPECIFIC_SNP =
#######################################################################
Digestion Hi-C
#######################################################################
GENOME_FRAGMENT = /home/genome/Caulobacter/bacteria_dpnii.bed
LIGATION_SITE = AAGCTAGCTT
MIN_FRAG_SIZE =
MAX_FRAG_SIZE =
MIN_INSERT_SIZE =
MAX_INSERT_SIZE =
#######################################################################
Hi-C processing
#######################################################################
MIN_CIS_DIST =
GET_ALL_INTERACTION_CLASSES = 1
GET_PROCESS_SAM = 0
RM_SINGLETON = 1
RM_MULTI = 1
RM_DUP = 1
#######################################################################
Contact Maps
#######################################################################
#BIN_SIZE = 20000 40000 100000 150000 500000 1000000
BIN_SIZE = 100000
MATRIX_FORMAT = upper
#######################################################################
Normalization
#######################################################################
MAX_ITER = 100
FILTER_LOW_COUNT_PERC = 0.02
FILTER_HIGH_COUNT_PERC = 0
EPS = 0.1
Could you kindhearted help me to fix this problem?
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