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Hi Christpher,Would you help me out? Thanks. See below for details.
On Thu, Mar 19, 2020 at 5:01 PM MAOMAO wrote:
Hi Dr. Chang,--I am trying to change family ID to 0 in .ped file, but it gives me an error: awk: program limit exceeded: maximum number of fields size=32767 FILENAME="merged_clean1.ped" FNR=1 NR=1awk '{$1 = "0"; print}' merged_clean1.ped > change.ped I am not sure how to fix it. However, it works when Iuse awk '{$1 = "0"; print}' merged_clean1.fam > change.famMy .ped file looks like below1 2002034 0 0 1 0 A C C A T .......2 2009036 0 0 1 0 A T A T T ......3 2000349 0 0 2 0 T A T C A ..........The reason I change FID to 0, because I have 3 plates samples and each one assign the FID as consecutive number from 1 to 96. When I do the duplicate check use --genome --rel-check, the PI-HAT all less than 0.4. It was supposed to have a couple of duplicates.Would you give me some suggestions?Thanks in advance!MAOMAOOn Friday, April 5, 2019 at 5:54:12 PM UTC-4, Christopher Chang wrote:If you want to keep one sample in each group, you have to use your own script to modify the .fam file to assign unique IDs; otherwise plink has no way to know which sample in each duplicate group to keep.(plink 2.0 allows for an optional "source ID" field to distinguish multiple samples from the same individual, which is respected by --keep/--remove/etc. But the FID+IID+SID combination is still required to be unique there.)
On Friday, April 5, 2019 at 2:46:47 PM UTC-7, fasssster101 wrote:Hello,My apologizes if this has already been answered... I am trying to update my *.bed, *.bim, and *.fam files by removing duplicate samples (not snps). These are individuals with the same FID and IID.I don't see an option in plink to do this ... ? If I use either the --keep or --remove option, how do I ensure that only one of the two duplicates are removed?Thank you!
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Hi Christpher,
Thanks for your reply.
I still have some questions:
1)do family ID really affect the IBD output? I am trying to identify the duplicates in my sample. However there are no duplicates there, all the PI-HAT value from 0 to 0.4. (it was supposed to have four duplicates.) I am thinking whether the problem is from family ID, because family ID is arranged by consecutive numbers(1,2,…,96) for each sample plate. After merging them, the family ID is all from 1 to 96, so I am trying to change all family ID to “0”.
If it works with .fam files, but how can I use –bfile including the .bed file to check duplicates? Or any easy way to do?
2)And do all the research need to check heterozygosity? When I check SNPs to prune SNPs, I want to exclude high inversion regions, how can I generate a list of that.
3)I use the plink1.9 and with the option --check-sex to check sex discrepancy, there are 4% of discrepancy. (16 of 400 samples). Is any way to check whether 4% is acceptable or within expected error?
Thanks in advance.
MAOMAO
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Hi Christpher,
Thanks for your reply.
I still have some questions:
1)do family ID really affect the IBD output? I am trying to identify the duplicates in my sample. However there are no duplicates there, all the PI-HAT value from 0 to 0.4. (it was supposed to have four duplicates.) I am thinking whether the problem is from family ID, because family ID is arranged by consecutive numbers(1,2,…,96) for each sample plate. After merging them, the family ID is all from 1 to 96, so I am trying to change all family ID to “0”.
If it works with .fam files, but how can I use –bfile including the .bed file to check duplicates? Or any easy way to do?
2)And do all the research need to check heterozygosity? When I check SNPs to prune SNPs, I want to exclude high inversion regions, how can I generate a list of that.
3)I use the plink1.9 and with the option --check-sex to check sex discrepancy, there are 4% of discrepancy. (16 of 400 samples). Is any way to check whether 4% is acceptable or within expected error?
Thanks in advance.
MAOMAO
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Hi Chrispher,
Thanks for your answers and help.
I have resolved two of them, but still have one not figured out. I tried to identify the sample duplicates (it is supposed to have 4 there), but it did not work. The PH-HAT still all less than 0.4. (attached is the .log file and part of plink.genome file) I have already changed all the family ID to 0. All the paternal and maternal ID are 0’s. Is that the problem? How to figure out? Any suggestion?
Thanks a lot!
Maomao
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Hi Christopher,
When I try to remove the identified duplicates, the command is: plink1.9 --bfile raw3 --remove duplicatesIDs.txt --make-bed --out sub_raw3 or plink1.9 --file raw3 --remove duplicatesIDs.txt --make-bed --out sub_raw3), both of them do not remove the duplicates and also the output does not give me any error. The sample size is still the same. I am not sure where’s the problem? Would you give me some suggestions? Thanks.
Here is the duplicatesIDs.txt
165 00003568M1
168 00003568M1_RE
174 00003568N1
178 00003568N1_RE
Best,
maomao
Hi Christopher,
When I try to remove the identified duplicates, the command is: plink1.9 --bfile raw3 --remove duplicatesIDs.txt --make-bed --out sub_raw3 or plink1.9 --file raw3 --remove duplicatesIDs.txt --make-bed --out sub_raw3), both of them do not remove the duplicates and also the output does not give me any error. The sample size is still the same. I am not sure where’s the problem? Would you give me some suggestions? Thanks.
Here is the duplicatesIDs.txt
165 00003568M1
168 00003568M1_RE
174 00003568N1
178 00003568N1_RE
Best,
maomao
On Mon, Mar 23, 2020 at 2:54 PM Ying Zhao wrote:
Thanks so much Christpher. It works. :)
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Hi Christopher,Here is my log
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Hi Christopher,I check my .fam file and they are matching the IDs. The family ID and sample ID I want to remove are the same. The command did not give me an error, but it did not actually remove anything.
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